RN Part-time
Cleveland Clinic

Research Nurse Coordinator - Clinical Research Unit

Cleveland Clinic Cleveland, OH
At Cleveland Clinic Health System, we believe in a better future for healthcare. And each of us is responsible for honoring our commitment to excellence, pushing the boundaries and transforming the patient experience, every day. We all have the power to help, heal and change lives — beginning with our own. That’s the power of the Cleveland Clinic Health System team, and The Power of Every One. Job Title Research Nurse Coordinator - Clinical Research Unit Location Cleveland Facility Cleveland Clinic Main Campus Department LRI M51 Clinical Research Unit-Research Innov and Educ Job Code F24020 Shift Days Schedule 6:30am-5:00pm Job Summary Job Details Join Cleveland Clinic’s Main Campus where research and surgery are advanced, technology is leading-edge, patient care is world class and caregivers are family. Here, you will work alongside a passionate and dedicated team, receive endless support and appreciation, and build a rewarding career with one of the most respected healthcare organizations in the world. Cleveland Clinic’s M51 Clinical Research Unit has a culture that sets it apart. This unit serves as a centralized research resource for clinical trials across Cleveland Clinic, supporting studies from a wide range of institutes and providing caregivers with valuable exposure to the enterprise, extensive networking opportunities, and pathways for professional growth and advancement. As a Research Nurse Coordinator, you will coordinate the implementation and conduct of human subject research projects by utilizing the nursing process while ensuring adherence to research protocols, regulatory requirements, and patient safety standards. In this role, you will provide specialized research nursing services, including laboratory specimen collection, EKGs, IV infusions, oral medication administration, adverse event management, and patient monitoring during study visits. Supporting both adult and pediatric participants, you will play a key role in Phase I and other clinical trials, helping ensure research participants are safely monitored while contributing to groundbreaking discoveries that advance patient care. A caregiver in this role works days from 6:30 a.m. – 5:00 p.m. A caregiver who excels in this role will: Coordinate the implementation and conduct of research projects ensuring adherence to research protocol requirements, timely completion and communication of regulatory documents, the development of data capture and monitoring plans. Serve as a liaison between investigators, research personnel, outside study personnel and central research administration offices to assist in protocol interpretation, enrollment and safety questions. Utilize the nursing process as a basis for patient care. Assess research subjects and complete nursing assessment, documenting findings in research subject records. Notify physicians of abnormal findings. Establish a care plan in collaboration with the research subject, family and research team. Coordinate ongoing care. Identify discharge needs and facilitate discharge planning as appropriate. Perform telephone triage. Perform nursing procedures and treatments as directed by physician or LIP in the treatment and management of patient care. Evaluate, initiate and maintain standards of care consistent with CCHS policies and procedures. Assist with specialized patient care equipment as required by the clinical research protocol. Administer medications and treatments as ordered by a physician or LIP. Direct, coordinate and participate in the evaluation and supervision of nursing care provided to research subjects; establishing patient care priorities and delegating nursing activities according to the patient’s needs and staff qualifications and capabilities. Participate in education, research and performance improvement activities. Develop and maintain knowledge of research protocol to coordinate the comprehensive and compliant execution of assigned protocols. Assist with preparation for audits and response to audits. Maintain professional relationships, including frequent and open effective communication with internal and external constituents. Assist with the development of training and educational material for assigned research protocols. Provide and document education as needed. Develop protocol specific checklists. Educate the patient/family and team on the research protocol. Conduct and document the informed consent process. May Assist PI with research study design and development of the research protocol. May assist with research project budget development. Perform other duties as assigned. Minimum qualifications for the ideal future caregiver include: Graduate from an accredited school of professional nursing Current state licensure as a Registered Nurse (RN) Basic Life Support (BLS) Certification through the American Heart Association (AHA) or American Red Cross Basic computer proficiency Four years of clinical experience Two years of research experience Understanding of the research process and terminology In-depth knowledge of the specialty under investigation Working knowledge of federal regulations and good clinical practice (GCP) Preferred qualifications for the ideal future caregiver include: Bachelor’s of Science in Nursing (BSN) Physical Requirements: Requires full range of body motion, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extended periods of time. Requires corrected vision and hearing to normal range. Requires working under stressful conditions and irregular hours. Exposure to communicable diseases and/or body fluids. Sedentary Work - Exerting up to 10 pounds of force occasionally (Occasionally: activity or condition exists up to 1/3 of the time) and/or a negligible amount of force frequently (Frequently: activity or condition exists from 1/3 to 2/3 of the time) to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time, but may involve walking or standing for brief periods of time. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met. Personal Protective Equipment: Follows standard precautions using personal protective equipment as required. The policy of Cleveland Clinic Health System and its system hospitals (Cleveland Clinic Health System) is to provide equal opportunity to all of our caregivers and applicants for employment in our drug free environment. All offers of employment are followed by testing for controlled substances. Cleveland Clinic Health System administers an influenza prevention program. You will be required to comply with this program, which will include obtaining an influenza vaccination on an annual basis or obtaining an approved exemption. Decisions concerning employment, transfers and promotions are made upon the basis of the best qualified candidate without regard to color, race, religion, national origin, age, sex, sexual orientation, marital status, ancestry, status as a disabled or Vietnam era veteran or any other characteristic protected by law. Information provided on this application may be shared with any Cleveland Clinic Health System facility. If applying for a Florida position, please see the following website for more information on the background screening requirements required by the Agency of Health Care Administration: https://info.flclearinghouse.com/ Please review the Equal Employment Opportunity poster . Cleveland Clinic is pleased to be an equal employment opportunity employer.
RN Full-time
OSF HealthCare

Coordinator Clinical Research RN

OSF HealthCare Peoria, IL
Total Rewards "Your life - our Mission" OSF HealthCare is dedicated to provide Mission Partners with a comprehensive and market-competitive total rewards package that includes benefits, compensation, recognition and well-being offerings that focus on the whole person and engage with their current stage of life and career. Click here to learn more about benefits and the total rewards at OSF. Pay range for this position is $34.25 - $51.13/hour. Actual pay is based on years of licensure. This is a Salaried position. Overview POSITION SUMMARY: The Clinical Research Coordinator RN (CRC) is a specialized research professional working with, and under the direction of a clinical Principal Investigator (PI). While the PI is primarily responsible for the overall design, conduct, and management of the research project/trial, the CRC reviews and comprehends the protocol and supports, facilitates, and coordinates the daily clinical research/trial activities and plays a critical role in the conduct of the study. The CRC plans, directs, and coordinates all aspects of research projects. CRC is responsible for assuring research is conducted in an ethical manner, using Good Clinical Practice (GCP). CRC’s are responsible for both clinical and administrative/business functions relating to their assigned projects. CRC’s play a critical liaison/connector role between study team, department leadership, Institution, and Sponsors Qualifications REQUIRED QUALIFICATIONS: License/Certifications: Current American Heart Association HealthCare Provider CPR Certification is required prior to start date of employment. Experience: 2 years experience as an RN Proficient in Microsoft Word, Excel, Power Point, and general computer proficiency required. Strong organization skills: ability to multi-task, prioritize and meet deadlines. Must demonstrate attention to detail and accuracy, time management skills, and proven ability to successfully follow-through on multiple, assigned projects. Professional and effective verbal and written communication skills and strong interpersonal skills, with the ability to work and communicate with various individuals within and external to the organization. Licensure/Certifications: Current Illinois RN licensure PREFERRED QUALIFICATIONS: Education: BSN Master’s degree in clinical research, healthcare, nursing, sciences, business, or related field Experience: 3-4 years direct research experience in a study coordinator role In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i.e., International Conference on Harmonization (ICH), Good Clinical Practice (GCP) and CFR 21. 1 year phlebotomy experience Licensure/Certifications: Collaborative Institutional Training Initiative (CITI) Training Course Certificates: Human Subject Protection (HSP), Good Clinical Practice (GCP), Responsible Conduct of Research (RCR), Conflict of Interest (COI) Certified Clinical Research Coordinator (CCRC) and/or Certified Clinical Research Professional (CCRP) International Air Transport Association (IATA) – Shipping of Dangerous Goods certification from Mayo Clinic OSF HealthCare is an Equal Opportunity Employer.
RN Other
MaineHealth

Lead Clinical Research Nurse Coordinator (RN)

MaineHealth Scarborough, ME
Description MaineHealth Institute for Research Nursing Req #: 76029 Summary This position is for someone interested in joining a hands-on team at theMHIR - MaineHealth Institute for Research, which is contributing to biomedical research in the area of Oncology. Our team is specifically interested in therapeutic trials, testing various combinations of chemotherapy, immunotherapy, targeted therapy, and radiation therapy.This Lead Clinical Research Nurse Coordinator will work at the direction of the Manager,Clinical Trials Office, and will be responsible forall aspects of research coordination, actively pre-screening and enrolling patients, scheduling study assessments, clinical data management, and communication with the study sponsor. This includes collaboration with thePrincipal Investigator, Program Coordinator, Study Center, and relevant MaineHealth Departments. The primary responsibilities includestudy coordination and acting as a hospital educator/resource person for studies. The primary characteristics of a successful Lead Clinical Research Nurse Coordinator include supervisory skills, attention to detail, highly organized, and excellent communication skills.This position plays a lead role in training and ongoing operations support of other Clinical Research Nurse Coordinators A hybrid work schedule from our Scarborough, Maine location is available for this position. Some reimbursed travel to trial sites in Brunswick and Rockport will be required. The MaineHealth application, a cover letter and a resume or CV are all required elements for application to this position. Learn more about the MaineHealth Institute for Researchin this short video! Required Minimum Knowledge, Skills, And Abilities (KSAs) Education: Bachelor's Degree in a health science field required. Master’s degree preferred. License/Certifications: Current applicable state license as a Registered Nurse required. Experience: Two years of clinical experience in a healthcare setting required. Hiring Scam Alert MaineHealth will never request financial information during the interview or pre-hiring process. All legitimate communications will come from an email address ending in @mainehealth.org. If you suspect fraudulent activity, please report it immediately to mhcareers@mainehealth.org. Additional Information With a career at any of the MaineHealth locations across Maine and New Hampshire, you’ll be working with health care professionals that truly value the people around them – both within the walls of the organization and the communities that surround it. We offer benefits that support an individual's needs for today and flexibility to plan for tomorrow – programs such as paid parental leave, a flexible work policy, student loan assistance, training and education, along with well-being resources for you and your family. MaineHealth remains focused on investing in our care team and developing an inclusive environment where you can thrive and feel supported to realize your full potential. If you’re looking to build a career in a place where people help one another deliver best-in-class care, apply today. If you have questions about this role, please contact sharon.nightingale@mainehealth.org
RN Full-time
Lancaster General Health

Registered Nurse Clinical Research Coordinator (Full Time/Days)

Lancaster General Health Lancaster, PA
Description Penn Medicine is dedicated to our tripartite mission of providing the highest level of care to patients, conducting innovative research, and educating future leaders in the field of medicine. Working for this leading academic medical center means collaboration with top clinical, technical and business professionals across all disciplines. Today at Penn Medicine, someone will make a breakthrough. Someone will heal a heart, deliver hopeful news, and give comfort and reassurance. Our employees shape our future each day. Are you living your life's work? LOCATION: Lancaster, PA HOURS: Full Time (40 hours per week). Monday-Friday (8am-4:30pm). No nights or weekends. Position Summary: Plans, initiates, coordinates, implements, and oversees clinical trials within the LGHealth Research Institute under the direction of the clinical Principal Investigator PI who is responsible for the overall conduct and management of the clinical trial. Coordinates the daily clinical trial activities and plays the critical lead role in the conduct of clinical studies in accordance with local, state, and federal regulations. Must display dedication, enthusiasm, commitment, confidentiality, and flexibility with cross coverage of sites and with on-call hours when required. Qualified individuals must have the ability with or without reasonable accommodation to perform the following duties: Plans and coordinates assigned research studies, serves as principle liaison for the project, interfaces with research subjects and collects research data, oversees administrative support, develops appropriate tools needed to conduct the research, and maintains record keeping systems and procedures. Performs nursing responsibilities as needed based on research study requirements. Ensures all research activities occur in compliance with guidelines for human subject protection research. Ensures all key personnel engaged in the research study have met training requirements. Serves as a resource to other research staff members regarding assigned clinical protocols. Monitors the progress of research activities; develops and maintains records of research activities, and prepares periodic and ad hoc reports, as required by investigators, management, sponsors, and or regulatory bodies. Ensures billing of study procedures to the appropriate funding source. Provides regulatory oversight for the conduct of assigned clinical trials. Prepares and oversees LG Hospital IRB submissions and continuing reviews, maintains regulatory and legal documents per IRB, FDA, DOH and other applicable regulatory agencies when required. Develops and implements recruitment strategies in accordance with sponsor requirements. Oversees and conducts informed consent process under direction of Primary Investigator and maintains appropriate documentation according to GCP, FDA, and IRB guidelines. Maintains adequate inventory of study supplies. Oversees and maintains drug and medical device accountability according to regulatory guidelines for receipt, storage, dispensation, and return of investigational product according to SOPs policy on Investigational Drug Device Accountability. Collaborates with other Research Coordinators, particularly in areas where clinical and non-clinical research areas interface. Contributes to the mentoring of new research staff. Functions as a resource for physicians, other health care providers, and ancillary support staff regarding care of the research participant as it relates to any given clinical research protocol; conducts staff in-services as appropriate. Coordinates and manages the patient assessments according to protocol standards at LGHealth locations, in a clinically safe and regulatory compliant manner. Utilizes clinical knowledge and assessment skills necessary to evaluate, report, and record accurate medical information including response to therapy according to approved research protocol. Develops and maintains rapport with patients to promote adherence to treatment and data collection protocols. Coordinates participant tests and procedures and maintains study timelines in data collection and completion of case report forms. Assures collected data for any approved research protocol is correct, sufficient, all inclusive, regulatory compliant and the integrity is intact. Maintains study files in accordance with sponsor requirements and LGH SOP Policies, including consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms. Assures the source documentation of all research activities is completed and accessible for CRF completion, reporting purposes, and for site visits by Sponsors and other regulatory agencies. Facilitates, conducts and oversees monitoring visits with Sponsors and other related agencies for the purpose of evaluating the accuracy and quality of the collected data. Maintains effective and ongoing communication with Sponsor, research participants and PI during the course of the study. Other duties as assigned. Minimum Required Qualifications: Current license as a Registered Nurse, issued by the PA State Board of Nursing. Bachelor's degree in nursing OR Bachelor's degree in related field AND Associate Nursing degree. Two years’ experience in a research or clinical environment. Working knowledge of medical and research terminology. Comprehension of Federal Regulations for Human Subjects in research. Computer Competency including proficiency in Microsoft Outlook, Word, Excel, electronic data capture and electronic health records EHR navigation. Preferred Qualifications: Comprehension and certification in Good Clinical Practices ICH GCP for human research. Research professional certification CCRP or willingness to pursue certification. #LI-LJ1 We believe that the best care for our patients starts with the best care for our employees. Our employee benefits programs help our employees get healthy and stay healthy. We offer a comprehensive compensation and benefits program that includes one of the finest prepaid tuition assistance programs in the region. Penn Medicine employees are actively engaged and committed to our mission. Together we will continue to make medical advances that help people live longer, healthier lives. Live Your Life's Work We are an Equal Opportunity employer. Candidates are considered for employment without regard to race, ethnicity, color, sex, sexual orientation, gender identity, religion, national origin, ancestry, age, disability, marital status, familial status, genetic information, domestic or sexual violence victim status, citizenship status, military status, status as a protected veteran or any other status protected by applicable law.
RN Full-time
Penn Medicine

Registered Nurse Clinical Research Coordinator (Full Time/Days)

Penn Medicine Lancaster, PA
Description Penn Medicine is dedicated to our tripartite mission of providing the highest level of care to patients, conducting innovative research, and educating future leaders in the field of medicine. Working for this leading academic medical center means collaboration with top clinical, technical and business professionals across all disciplines. Today at Penn Medicine, someone will make a breakthrough. Someone will heal a heart, deliver hopeful news, and give comfort and reassurance. Our employees shape our future each day. Are you living your life's work? LOCATION: Lancaster, PA HOURS: Full Time (40 hours per week). Monday-Friday (8am-4:30pm). No nights or weekends. Position Summary: Plans, initiates, coordinates, implements, and oversees clinical trials within the LGHealth Research Institute under the direction of the clinical Principal Investigator PI who is responsible for the overall conduct and management of the clinical trial. Coordinates the daily clinical trial activities and plays the critical lead role in the conduct of clinical studies in accordance with local, state, and federal regulations. Must display dedication, enthusiasm, commitment, confidentiality, and flexibility with cross coverage of sites and with on-call hours when required. Qualified individuals must have the ability with or without reasonable accommodation to perform the following duties: Plans and coordinates assigned research studies, serves as principle liaison for the project, interfaces with research subjects and collects research data, oversees administrative support, develops appropriate tools needed to conduct the research, and maintains record keeping systems and procedures. Performs nursing responsibilities as needed based on research study requirements. Ensures all research activities occur in compliance with guidelines for human subject protection research. Ensures all key personnel engaged in the research study have met training requirements. Serves as a resource to other research staff members regarding assigned clinical protocols. Monitors the progress of research activities; develops and maintains records of research activities, and prepares periodic and ad hoc reports, as required by investigators, management, sponsors, and or regulatory bodies. Ensures billing of study procedures to the appropriate funding source. Provides regulatory oversight for the conduct of assigned clinical trials. Prepares and oversees LG Hospital IRB submissions and continuing reviews, maintains regulatory and legal documents per IRB, FDA, DOH and other applicable regulatory agencies when required. Develops and implements recruitment strategies in accordance with sponsor requirements. Oversees and conducts informed consent process under direction of Primary Investigator and maintains appropriate documentation according to GCP, FDA, and IRB guidelines. Maintains adequate inventory of study supplies. Oversees and maintains drug and medical device accountability according to regulatory guidelines for receipt, storage, dispensation, and return of investigational product according to SOPs policy on Investigational Drug Device Accountability. Collaborates with other Research Coordinators, particularly in areas where clinical and non-clinical research areas interface. Contributes to the mentoring of new research staff. Functions as a resource for physicians, other health care providers, and ancillary support staff regarding care of the research participant as it relates to any given clinical research protocol; conducts staff in-services as appropriate. Coordinates and manages the patient assessments according to protocol standards at LGHealth locations, in a clinically safe and regulatory compliant manner. Utilizes clinical knowledge and assessment skills necessary to evaluate, report, and record accurate medical information including response to therapy according to approved research protocol. Develops and maintains rapport with patients to promote adherence to treatment and data collection protocols. Coordinates participant tests and procedures and maintains study timelines in data collection and completion of case report forms. Assures collected data for any approved research protocol is correct, sufficient, all inclusive, regulatory compliant and the integrity is intact. Maintains study files in accordance with sponsor requirements and LGH SOP Policies, including consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms. Assures the source documentation of all research activities is completed and accessible for CRF completion, reporting purposes, and for site visits by Sponsors and other regulatory agencies. Facilitates, conducts and oversees monitoring visits with Sponsors and other related agencies for the purpose of evaluating the accuracy and quality of the collected data. Maintains effective and ongoing communication with Sponsor, research participants and PI during the course of the study. Other duties as assigned. Minimum Required Qualifications: Current license as a Registered Nurse, issued by the PA State Board of Nursing. Bachelor's degree in nursing OR Bachelor's degree in related field AND Associate Nursing degree. Two years’ experience in a research or clinical environment. Working knowledge of medical and research terminology. Comprehension of Federal Regulations for Human Subjects in research. Computer Competency including proficiency in Microsoft Outlook, Word, Excel, electronic data capture and electronic health records EHR navigation. Preferred Qualifications: Comprehension and certification in Good Clinical Practices ICH GCP for human research. Research professional certification CCRP or willingness to pursue certification. #LI-LJ1 We believe that the best care for our patients starts with the best care for our employees. Our employee benefits programs help our employees get healthy and stay healthy. We offer a comprehensive compensation and benefits program that includes one of the finest prepaid tuition assistance programs in the region. Penn Medicine employees are actively engaged and committed to our mission. Together we will continue to make medical advances that help people live longer, healthier lives. Live Your Life's Work We are an Equal Opportunity employer. Candidates are considered for employment without regard to race, ethnicity, color, sex, sexual orientation, gender identity, religion, national origin, ancestry, age, disability, marital status, familial status, genetic information, domestic or sexual violence victim status, citizenship status, military status, status as a protected veteran or any other status protected by applicable law.
RN Full-time
Cleveland Clinic

Research Nurse Coordinator

Cleveland Clinic Cleveland, OH
At Cleveland Clinic Health System, we believe in a better future for healthcare. And each of us is responsible for honoring our commitment to excellence, pushing the boundaries and transforming the patient experience, every day. We all have the power to help, heal and change lives — beginning with our own. That’s the power of the Cleveland Clinic Health System team, and The Power of Every One. Job Title Research Nurse Coordinator Location Cleveland Facility Cleveland Clinic Main Campus Department Research Administration-Research Innov and Educ Job Code T26103 Shift Days Schedule 8:00am-4:30am Job Summary Job Details Join Cleveland Clinic’s Main Campus where research and surgery are advanced, technology is leading-edge, patient care is world class and caregivers are family. Here, you will work alongside a passionate and dedicated team, receive endless support and appreciation, and build a rewarding career with one of the most respected healthcare organizations in the world. As a Research Nurse Coordinator in Rheumatology, you will help advance innovative clinical research by coordinating and managing human subject research studies from start-up through completion. In this role, you will protect the rights and welfare of research participants, evaluate protocol feasibility, prepare study sites for conduct, manage study activities, maintain regulatory documentation, and ensure accurate data collection and entry. You will collaborate closely with physicians, nurses, sponsors, and research partners while coordinating disease-specific clinical trials and supporting a growing CAR-T research portfolio. Responsibilities also include participant recruitment and consent, specimen collection and processing for the biorepository, administration of study-related injections and infusions, communication with sponsors, and working alongside multidisciplinary teams to ensure successful study execution and compliance with regulatory requirements. A caregiver in this role works days from 8:00 a.m. – 4:30 p.m. (flexible start/end times) A caregiver who excels in this role will: Coordinate the implementation and conduct of research projects, ensuring adherence to research protocol requirements and timely completion. Complete and communicate regulatory documents, develop data and monitoring plans, report Serious Adverse Events as they occur, and complete FDA and sponsor forms. Serve as a liaison between investigators, research personnel, outside study personnel, and central research administration offices to assist in protocol interpretation, enrollment, and safety questions. Assess research subjects, complete nursing assessments, document findings in research subject records, and notify the physician of abnormal findings. Establish a care plan in collaboration with the research subject, family, and research team, and coordinate ongoing care. Identify discharge needs and facilitate discharge planning as appropriate. Perform telephone triage, nursing procedures, and treatments. Evaluate, initiate, and maintain standards of care consistent with CCHS policies and procedures. Assist with specialized patient care equipment as required by the clinical research protocol. Administer medications and treatments as ordered by a physician or licensed independent provider (LIP). Direct, coordinate, and participate in the evaluation and supervision of nursing care provided to research subjects, establishing patient care priorities and delegating nursing activities according to patient needs and staff capabilities. Participate in education, research and performance improvement activities. Develop and maintain knowledge of research protocol to coordinate the comprehensive and compliant execution of assigned protocols. Assist with preparation for audits and response to audits. Maintain professional relationships, including frequent and open effective communication with internal and external constituents. Assist with the development of training and educational material for assigned research protocols. Provide and document education as needed. Conduct and document the informed consent process. Assist with research study design, development of research protocol and research project budget development. Other duties as assigned. Minimum qualifications for the ideal future caregiver include: Graduate from an accredited school of professional nursing Current state licensure as a Registered Nurse (RN) Basic Life Support (BLS) Certification through the American Heart Association (AHA) or American Red Cross Four years of clinical experience Two years of research experience Understanding of the research process and terminology In-depth knowledge of the specialty under investigation Working knowledge of federal regulations and good clinical practice (GCP) Preferred qualifications for the ideal future caregiver include: Bachelor’s of Science in Nursing (BSN) Ability to apply learning in real-life scenarios Ability to independently drive tasks to completion with minimal supervision Physical Requirements: Requires full range of body motion, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extended periods of time. Requires corrected vision and hearing to normal range. Requires working under stressful conditions and irregular hours. Exposure to communicable diseases and/or body fluids. Medium Work - Exerting 20 to 50 pounds of force occasionally, and/or 10 to 25 pounds of force frequently, and/or greater than negligible up to 10 pounds of force constantly to move objects. Physical Demand requirements are in excess of those for Light Work. Personal Protective Equipment: Follows standard precautions using personal protective equipment as required. The policy of Cleveland Clinic Health System and its system hospitals (Cleveland Clinic Health System) is to provide equal opportunity to all of our caregivers and applicants for employment in our drug free environment. All offers of employment are followed by testing for controlled substances. Cleveland Clinic Health System administers an influenza prevention program. You will be required to comply with this program, which will include obtaining an influenza vaccination on an annual basis or obtaining an approved exemption. Decisions concerning employment, transfers and promotions are made upon the basis of the best qualified candidate without regard to color, race, religion, national origin, age, sex, sexual orientation, marital status, ancestry, status as a disabled or Vietnam era veteran or any other characteristic protected by law. Information provided on this application may be shared with any Cleveland Clinic Health System facility. If applying for a Florida position, please see the following website for more information on the background screening requirements required by the Agency of Health Care Administration: https://info.flclearinghouse.com/ Please review the Equal Employment Opportunity poster . Cleveland Clinic is pleased to be an equal employment opportunity employer.
RN Pediatric Outpatient Full-time
Washington University Physicians

RN Research Nurse Coordinator I - Pediatric Clinical Research Unit (PCRU)

Washington University Physicians St. Louis, MO
$56,200 - $96,100 / year
Scheduled Hours 40 Position Summary Join a dedicated and dynamic team committed to advancing pediatric health. This position is in the Pediatric Clinical Research Unit (PCRU), an outpatient research unit located at St Louis Children’s Hospital. It is primarily a weekday and daytime position. Position performs duties associated with the coordination and implementation of research studies including direct patient care, data collection and management of data generated by study protocols. Job Description Primary Duties & Responsibilities: Works under the Principal Investigator’s (PI) guidance to meet the research objectives of the studies. Provides direct patient care in accordance with protocol and patient safety, including but not limited to, patient assessments, phlebotomy, IV placement, infusion monitoring, accessing/de-accessing ports, injections, ECGs, vital signs, and other nursing skills. Administers and provides oversight of administration of medications, investigational products, and study interventions, as appropriate. Obtains, handles, processes and ships research specimens according to protocol. Collects health information including monitoring for and reporting of adverse events. Performs data collection, source documentation, and data entry. Works with research team to: identify, screen and enroll study subjects; coordinate study procedures; and maintain continuity of care, human subject protection and research integrity. Collaborates with sponsor’s research associates during monitoring activities by providing study documentation, data clarifications and reports as necessary. Performs other duties incidental to the work described above. Working Conditions: Job Location/Working Conditions Normal office environment Exposure to blood-borne pathogens Requires protective devices Patient care setting Direct patient care setting Physical Effort Typically sitting at desk or table Typically standing or walking Typically bending, crouching, stooping Occasional lifting (25 lbs or less) Equipment Office equipment Clinical/diagnostic equipment The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel so classified. Management reserves the right to revise or amend duties at any time. Required Qualifications Education: A diploma, certification or degree is not required. Certifications /Professional Licenses : The list below may include all acceptable certifications, professional licenses and issuers. More than one credential, certification or professional license may be required depending on the role. Basic Life Support - American Heart Association, Basic Life Support - American Red Cross, Registered Nurse - Illinois Department of Financial and Professional Regulation, Registered Nurse - Missouri Division of Professional Registration Work Experience: No specific work experience is required for this position. Skills: Not Applicable Driver's License: A driver's license is not required for this position. More About This Job Required Qualifications: Graduate of an accredited nursing program. Current RN licensure in the state of Missouri and/or Illinois, depending on location. Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirements). Preferred Qualifications Education: B.S. - Bachelor of Science - Nursing, B.S.N. - Bachelor of Science in Nursing Certifications /Professional Licenses : No additional certification/professional licenses unless stated elsewhere in the job posting. Work Experience: Clinical Research (1 Year) Skills: Clinical Research, Clinical Research Coordination, Clinical Research Management, Clinical Research Methods, Clinical Research Operations, Clinical Techniques, Critical Thinking, Database Management, Effective Written Communication, Electronic Health Records (EHR), Interpersonal Relationships, Nursing Fundamentals, Oral Communications, Patient Recruitment, Phlebotomy, Spreadsheet Software, Statistical Analysis Software (SAS), Team Collaboration Grade S25 Salary Range $56,200.00 - $96,100.00 / Annually The salary range reflects base salaries paid for positions in a given job grade across the University. Individual rates within the range will be determined by factors including one's qualifications and performance, equity with others in the department, market rates for positions within the same grade and department budget. Questions For frequently asked questions about the application process, please refer to our External Applicant FAQ . Accommodation If you are unable to use our online application system and would like an accommodation, please email CandidateQuestions@wustl.edu or call the dedicated accommodation inquiry number at 314-935-1149 and leave a voicemail with the nature of your request. All qualified individuals must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship. Pre-Employment Screening All external candidates receiving an offer for employment will be required to submit to pre-employment screening for this position. The screenings will include criminal background check and, as applicable for the position, other background checks, drug screen, an employment and education or licensure/certification verification, physical examination, certain vaccinations and/or governmental registry checks. All offers are contingent upon successful completion of required screening. Benefits Statement Personal Up to 22 days of vacation, 10 recognized holidays, and sick time. Competitive health insurance packages with priority appointments and lower copays/coinsurance. Take advantage of our free Metro transit U-Pass for eligible employees. WashU provides eligible employees with a defined contribution (403(b)) Retirement Savings Plan, which combines employee contributions and university contributions starting at 7%. Wellness Wellness challenges, annual health screenings, mental health resources, mindfulness programs and courses, employee assistance program (EAP), financial resources, access to dietitians, and more! Family We offer 4 weeks of caregiver leave to bond with your new child. Family care resources are also available for your continued childcare needs. Need adult care? We’ve got you covered. WashU covers the cost of tuition for you and your family, including dependent undergraduate-level college tuition up to 100% at WashU and 40% elsewhere after seven years with us. For policies, detailed benefits, and eligibility, please visit: https://hr.wustl.edu/benefits/ EEO Statement Washington University in St. Louis is committed to the principles and practices of equal employment opportunity. It is the University’s policy to provide equal opportunity and access to persons in all job titles without regard to race, ethnicity, color, national origin, citizenship (where prohibited by federal law), age, religion, sex, sexual orientation, gender identity or expression, disability, protected veteran status, or genetic information.
RN Full-time
PeaceHealth

Clinical Research RN

PeaceHealth Bellingham, WA
$105,851 - $158,766 / year
Description Job Description Clinical Research RN – Make an Impact in Beautiful Bellingham, WA PeaceHealth | Full-Time | Day Shift | 1.0 FTE Are you a compassionate Registered Nurse with a passion for advancing patient care through research? At PeaceHealth , we believe clinical research is more than data—it’s about improving lives, shaping the future of healthcare, and honoring our mission of healing. Join our dedicated team in Bellingham, Washington , where your expertise as a Clinical Research RN will directly support innovative studies while guiding patients through meaningful healthcare journeys. Why You’ll Love This Role As a Clinical Research RN, you’ll be at the intersection of patient care and clinical innovation. You’ll collaborate closely with physicians, research teams, and study sponsors while building trusting relationships with patients participating in important clinical studies. This is an ideal role for a self-motivated nurse who enjoys autonomy, organization, and making a measurable difference beyond the bedside. What You’ll Do Partner with physicians to identify and recruit eligible patients for clinical research studies Guide participants through the informed consent process with empathy and clarity Coordinate all aspects of assigned studies, including data collection, documentation, and compliance Maintain accurate, audit-ready records and ensure adherence to Good Clinical Practice (GCP) standards Serve as a key liaison between patients, providers, and study sponsors Communicate effectively with diverse patient populations and interdisciplinary teams What You Bring Required Associate Degree in Nursing (BSN preferred) Active RN license in Washington Minimum 3 years of relevant nursing experience Strong organizational, critical thinking, and communication skills Ability to work independently and manage multiple priorities Preferred Clinical research experience Oncology certification (OCN) ACRP certification Familiarity with electronic health records and research databases Compensation & Benefits Annual Salary Range: $105,851 - $158,766 PeaceHealth is deeply committed to caregiver wellbeing. Our comprehensive benefits package supports you in every aspect of your life: Full medical, dental, and vision coverage 403(b) retirement plan with employer contributions and match Generous paid time off Employer-paid life and disability insurance Tuition assistance and continuing education reimbursement Expanded EAP and mental health support Robust wellness programs supporting physical, emotional, financial, social, and spiritual wellbeing About PeaceHealth PeaceHealth is a mission-driven, not-for-profit healthcare system dedicated to compassionate care and community wellbeing. Our culture is grounded in: Inclusivity and respect for diversity Cultural humility and belonging A commitment to supporting caregivers as whole people Here, you’ll find purpose, support, and a team that truly values your contributions. Life in Bellingham, Washington Located between Seattle and Vancouver, BC, Bellingham offers the best of the Pacific Northwest lifestyle: Easy access to mountains, forests, and the Puget Sound Abundant outdoor recreation including hiking, biking, kayaking, and skiing A vibrant local arts scene, farmers markets, and welcoming community culture A relaxed pace of life surrounded by natural beauty Whether you’re exploring scenic trails or enjoying waterfront views, Bellingham is an ideal place to live and work. Join Us If you’re ready to bring your nursing expertise into a dynamic research environment—and be part of a team that values compassion, curiosity, and excellence—we encourage you to apply. For full consideration, please include a current resume with your application. PeaceHealth is an EEO/AA Employer/Veterans/Disabled committed to equity and inclusion in all we do.
RN Outpatient Outpatient Full-time
University of Mississippi Medical Center (UMMC)

RN-Clinical Research - Clinic Research Support

University of Mississippi Medical Center (UMMC) Jackson, MS
Hello, Thank you for your interest in career opportunities with the University of Mississippi Medical Center. Please review the following instructions prior to submitting your job application: Provide all of your employment history, education, and licenses/certifications/registrations. You will be unable to modify your application after you have submitted it. You must meet all of the job requirements at the time of submitting the application. You can only apply one time to a job requisition. Once you start the application process you cannot save your work. Please ensure you have all required attachment(s) available to complete your application before you begin the process. Applications must be submitted prior to the close of the recruitment. Once recruitment has closed, applications will no longer be accepted. After you apply, we will review your qualifications and contact you if your application is among the most highly qualified. Due to the large volume of applications, we are unable to individually respond to all applicants. You may check the status of your application via your Candidate Profile. Thank you, Human Resources Important Applications Instructions: Please complete this application in entirety by providing all of your work experience, education and certifications/ license. You will be unable to edit/add/change your application once it is submitted. Job Requisition ID: R00051273 Job Category: Nursing Organization: RN Mgr-Clinical Research Operations Location/s: Main Campus Jackson Job Title: RN-Clinical Research - Clinic Research Support Job Summary: To coordinate and conduct research projects and related activities as assigned. To coordinate the recruitment, care and treatment of research participants in accordance with established study protocols and in accordance with FDA guidelines. To ensure adherence to applicable policies, procedures, standards, and practices. Education & Experience Education and Experience Required: Must be licensed as RN for two (2) years Certifications, Licenses or Registration required: Valid RN license. Knowledge, Skills & Abilities Knowledge, Skills, and Abilities: Knowledge of the principles and procedures of clinical research. Knowledge of FDA regulations. Verbal and written communication skills. Interpersonal skills to interact with a wide range of constituencies. Skill in the use of personal computers and related software applications. Ability to prepare and process laboratory samples using established protocols. Ability to draw blood, administer IVs and perform standard nursing procedures. Ability to maintain quality, safety, and/or infection control standards. Responsibilities Participates in coordinates the planning, development, and implementation of clinical protocols in accordance with established research parameters. Inputs data and maintains research databases and related records needed for research. Distributes research information to faculty, research staff, investigators, and others as requested. Oversees the planning, scheduling and implementation of daily clinical activities and procedures, ensuring adequate patient care and treatment. Ensures clinical activities are carried out in accordance with established research protocols, clinical procedures, and safety standards. Recruits and enrolls suitable candidate, ensuring required documentation is collected and processed. Provides basic background and education to participants. Administers prescribed medications, performs phlebotomy, monitors vital signs, and/or performs other specialized nursing procedures. The duties listed are general in nature and are examples of the duties and responsibilities performed and are not meant to be construed as exclusive or all-inclusive. Management retains the right to add or change duties at any time. Physical and Environmental Demands Requires frequent exposure to unpleasant or disagreeable physical environment such as high noise level and exposure to heat and cold, frequent handling or working with potentially dangerous equipment, frequent exposure to biohazardous conditions such as risk of radiation exposure, blood borne pathogens, fumes or airborne particles, and/or toxic or caustic chemicals which mandate attention to safety considerations, occasional working hours significantly beyond regularly scheduled hours, occasional travelling to offsite locations, occasional activities subject to significant volume changes of a seasonal/clinical nature, constant work produced subject to precise measures of quantity and quality, frequent bending, occasional lifting and carrying up to 50 pounds, frequent crouching/stooping, occasional driving, occasional kneeling, frequent pushing/pulling, frequent reaching, frequent sitting, frequent standing, frequent twisting, and frequent walking. (occasional-up to 20%, frequent-from 21% to 50%, constant-51% or more) Time Type: Full time FLSA Designation/Job Exempt: Yes Pay Class: Salary FTE %: 100 Work Shift: Day Benefits Eligibility: Grant Funded: Yes Job Posting Date: 07/2/2026 Job Closing Date (open until filled if no date specified):
RN Full-time
Atlantic Health System

Clinical Research Nurse Coordinator, full-time day 8a-4p, Medicine Research, Morristown

Atlantic Health System Morristown, NJ
$50.15 - $88.28 / hour
Job Description Responsible for coordinating and performing study specific clinical and regulatory activities across multiple study protocols of different therapeutic areas and phases, in accordance with appropriate regulations, Standard Operating Procedures (SOPs), and study specific protocols/plans and processes Principal Accountabilities Coordinates and implements the assigned protocols and recruit subjects to collect data from patient charts, medical records, interviews, questionnaires, diagnostic tests and other sources. Ensures compliance with protocol guidelines and requirements of regulatory agencies, identifies problems and/or inconsistencies and monitors patients' progress to include documentation and reporting of adverse events, and recommends corrective action as appropriate. Coordinates the development of forms, questionnaires and the application of research techniques, assists in writing procedure manuals, reviews journals, abstracts and scientific literature to keep abreast of new developments and to obtain information regarding previous studies to aid in planning. Develops appropriate regulatory reports and associated documentation in accordance with SOPs and study specific processes. Performs periodic regulatory audits on department studies being coordinated by other coordinators. Works closely with sponsor and study personnel on relevant safety and regulatory issues. Completes tasks within timeframe by appropriately prioritizing multiple tasks within or across studies and adapts to timeline or priority changes by reorganizing daily workload. Performs other related duties as assigned. Required QUALIFICATIONS Bachelor's degree in nursing or related field. Valid New Jersey Nursing License required. Minimum 5 Years of experience required in Oncology and/or Research Nursing or other relevant area. Preferred BLS an ACLS certification. CCRC certification preferred About Us At Atlantic Health, our promise to our communities is; Anyone who enters one of our facilities will receive the highest quality care delivered at the right time, at the right place, and at the right cost. This commitment is also echoed in the respect, development and opportunities we give to our more than 22,000 team members. Headquarters in Morristown, New Jersey, we are one of the leading non-profit health care systems in the nation. Our facilities and sites of care include: Atlantic Health Morristown Medical Center, Morristown, NJ Atlantic Health Overlook Medical Center, Summit, NJ Atlantic Health Newton Medical Center, Newton, NJ Atlantic Health Chilton Medical Center, Pompton Plains, NJ Atlantic Health Hackettstown Medical Center, Hackettstown, NJ Atlantic Health Goryeb Children's Hospital, Morristown, NJ Atlantic Health CentraState Healthcare System, Freehold, NJ Atlantic Medical Group Atlantic Visiting Nurse Atlantic Mobile Health Atlantic Rehabilitation We have more than 900 community-based healthcare providers affiliated through Atlantic Medical Group. We Have Received Awards And Recognition For The Services We Have Provided To Our Patients, Team Members And Communities. Below Are Just a Few Of Our Accolades Chosen for 17 years by Fortune as one of the magazine’s “100 Best Companies to Work For." Atlantic Health Morristown and Atlantic Health Overlook Named by Newsweek as two of the “World’s Best Hospitals” in 2026. Atlantic Health Morristown and Atlantic Health Overlook ranked within the top three hospitals in New Jersey by U.S. News & World Report’s 2025-2026 Best Hospital rankings. Atlantic Health scored four “A” grades by The Leapfrog Group in its Fall 2025 Hospital Safety Grades, performance measures reflecting errors, accidents, injuries and injections, as well as systems hospitals have in place to prevent harm. Atlantic Health Morristown and Atlantic Health Overlook are New Jersey's only hospitals to be named among America's 50 Best hospitals by Healthgrades in 2026. Named by Becker's Healthcare as one of the "165 Top Places to Work in Healthcare – 2026. Atlantic Health Morristown, Atlantic Health Overlook, Atlantic Health Chilton and Atlantic Health Newton all Forbes Top Hospitals for 2026. Named by Newsweek as one of America’s Greatest Workplaces for Inclusion & Diversity 2025. Atlantic Health rated LEVEL 9 - 2025 CHIME Digital Health Most Wired. Summary Atlantic Health offers a competitive and comprehensive Total Rewards package that supports the health, financial security, and well-being of all team members. Offerings vary based on role level (Team Member, Director, Executive). Below is a general summary, with role-specific enhancements highlighted: Team Member Benefits Medical, Dental, Vision, Prescription Coverage (22.5 hours per week or above for full-time and part-time team members) Life & AD&D Insurance. Short-Term and Long-Term Disability (with options to supplement) 403(b) Retirement Plan: Employer match, additional non-elective contribution PTO & Paid Sick Leave Tuition Assistance, Advancement & Academic Advising Parental, Adoption, Surrogacy Leave Backup and On-Site Childcare Well-Being Rewards Employee Assistance Program (EAP) Fertility Benefits, Healthy Pregnancy Program Flexible Spending & Commuter Accounts Pet, Home & Auto, Identity Theft and Legal Insurance ____________________________________________ Note: In Compliance with the NJ Pay Transparency Act (effective Sunday, June 1, 2025), all job postings will include the hourly wage or salary (or a range), as well as this summary of benefits. Final compensation and benefit eligibility may vary by role and employment status and will be confirmed at the time of offer. EEO STATEMENT Atlantic Health, Inc. is an equal employment opportunity employer and federal contractor or subcontractor and therefore abides by applicable laws to protect applicants and employees from discrimination in hiring, promotion, discharge, pay, fringe benefits, job training, classification, referral, and other aspects of employment, on the basis of race, color, religion, sex (including pregnancy, gender identity and sexual orientation), national origin, citizenship status, disability, age, genetics, or veteran
RN Full-time
McLaren Health Care

Clinical Research Registered Nurse

McLaren Health Care Detroit, MI
Department: Clinical Research (RN position - Detroit) Scheduled Bi-Weekly Hours: 80 Shift: Full-Time Days Daily Work Times: 7:30am-4:00pm Position Summary: The CRN is a member of the clinical research team and assists in the recruitment, compliance and follow-up of patients that are eligible for, or registered to a clinical trial. The CRN provides specialized nursing care that ensures exceptional, ethical, safe care yielding high-quality data. Responsible for managing patient standard of care needs as well as participant and protocol needs through application of independent judgment, communication and collaboration with the research patient, patient’s family, ancillary/support services, the physician, and the clinical research team. Responsibilities: Provides clinical trial support to ensure patients are offered appropriate clinical trials following Good Clinical Practice standards. Assesses, monitors, evaluates, and documents the patient’s compliance and response to protocol treatment Provides leadership to other members of the clinical team by articulating expected standards of care as directed by the clinical trial. Delegates and supervises other employees, as assigned, to ensure that the clinical trial plan is carried out and that established outcomes are achieved. Participates in process improvement activities of the department to ensure patient safety. Demonstrates professionalism and a commitment to improving the work environment through participation in meetings, timely and effective communication, and an embracement of cultural diversity Provides clinical research support staff with the documentation needed to determine eligibility and maintain compliance Required Associate Degree from an accredited Nursing program Current State of Michigan Registered Nurse license Two years of nursing experience Preferred Research experience in designated area of work Nursing experience in area of clinical research focus Additional Information Schedule: Full-time Requisition ID: 26003192 Daily Work Times: 7:30am-4:00pm Hours Per Pay Period: 80 On Call: No Weekends: No
RN Full-time
Temple Health

CLINICAL RESEARCH NURSE II

Temple Health Philadelphia, PA
Coordinate and facilitate the conduct of clinical research protocols which may be supported by NCI, industry, cooperative groups, or grant funded and investigator-initiated. Provide leadership in the management and operation of clinical research protocols to ensure research participant recruitment and accrual, protocol compliance, research participant safety and data quality. The position will work closely with the members of the clinical research team to develop effective tools for close monitor and reporting of trials accrual and coordinate the timely study activation and submission of protocol amendments. This position supports the Fox Chase Cancer Center Office of Clinical Research at Temple University Hospital, Main Campus or East Norriton and Buckingham Campuses. In addition, this position is expected to interact with the institutional investigators, other members of healthcare team, service line members and research participants/families in a manner, which supports the conduct of clinical trials. Flexibility in work schedule when possible, must be maintained to ensure coverage of study responsibilities. Education Bachelor's Degree Required Experience Master's Degree Preferred 2 Years Experience As a Clinical Research Nurse Required 2 years experience in nursing with a focus on oncology or comparable clinical environment Required 2 years experience with oncology or equivalent clinical trials Required General Experience and knowledge of chemotherapy administration and/or radiation therapy treatment modalities Preferred Licenses PA Registered Nurse License Required Oncology Nursing Cert Corp Preferred Cert Clin Research Prof Preferred or Cert Clin Research Coordinator Preferred Or Cert Clin Research Associate Preferred Multi State Compact RN License Required Or
RN Other
CentraCare

Clinical Research RN | Heart Center Research

CentraCare St. Cloud, MN
$41.92 - $64.18 / hour
Discover a rewarding career with CentraCare as a Clinical Research Registered Nurse (RN) in our innovative Heart & Vascular Center! Join an organization committed to improving the health of our communities through exceptional patient care and groundbreaking clinical research. In this role, you'll have the unique opportunity to contribute to studies that help shape the future of cardiovascular medicine while partnering with leading industry sponsors such as Boston Scientific and Medtronic. As a Clinical Research RN, you will collaborate with physicians, providers, and research teams to manage all phases of the nursing care process within clinical research studies- assessing/screening of patients, determining patient eligibility based on research study criteria, interpreting data, planning, implementing, and evaluating care and coordinating care with providers. If you are a compassionate RN who is passionate about clinical research, advancing medical knowledge, and delivering exceptional patient care, we encourage you to apply and become part of the CentraCare team. Schedule: Full-time | 64-80 hours every two weeks | Onsite-St. Cloud Hospital Days | 7:00am-4:00pm | Monday – Friday Pay and Benefits: Pay range: $41.92-$64.18; pay determined by experience Benefits : medical, dental, PTO, retirement, employee discounts and more! CentraCare is also proud to offer other perks such as free onsite parking, tuition assistance, scholarships, wellness program with rewards and employee discounts Qualifications: Graduate from an accredited nursing program required BSN or MSN preferred BSN or higher required within 36 months of being hired Current Minnesota RN License required Three years related experience preferred. Knowledge of nursing standards, policies, procedures, and ethics Experience with Microsoft Office Software Current American Heart Association (AHA) BLS Healthcare Provider card required National certification in a nursing specialty preferred. CentraCare has made a commitment to diversity in its workforce. All individuals including, but not limited to, individuals with disabilities, are encouraged to apply. CentraCare is an EEO/AA employer.
RN Oncology Other
Cone Health

Oncology Clinical Research RN

Cone Health Glen Raven, NC
Clinical Research Nurses work closely with study subjects and other research staff and are involved in most steps of the research trial process. They perform some patient-related care and assessments within the scope of their licensure. Their work is routine in nature, with assignments provided at a task level, focused on the long-term goals of clinical research trial and process. Clinical Research Nurses have no supervisory responsibilities and work under immediate supervision. Essential Job Function: Reviews patient cases, medical histories, and current treatment plans to effectively recruit and enroll potential research subjects that are actively engaged in the informed consent process. Supports the regulatory process in the submission of study protocols, consent forms, and recruiting materials to the Institutional Review Board and the department for approval, facilitating the regulatory compliance necessary for research projects in the hospital/medical group setting. Helps coordinate activities for multiple simultaneous clinical trials, managing various research tasks efficiently, ensuring optimal use of resources and executing research protocols in a timely manner. Serves as study coordinator for pharmaceutical and/or device trials, successfully coordinating site initiation visits, monitoring visits, and close-out visits, and ensuring adherence to protocol guidelines and regulatory requirements. Corresponds with healthcare teams, providers, outside research partners, and patients, ensuring clear communication and continuity of care for patients. Assists in collecting and Reviewing data specific to clinical research studies to ensure accuracy and reliability. Assists with the maintenance of records of patient interactions and clinical research interventions to ensure consistent and coordinated care, including collaborating with Investigator in assessment and management of Adverse Events. Completes clinical tasks within the scope of nursing license to meet patients' immediate needs as necessary. Coordinates patient care under direction of the Investigator and in accordance with the clinical trial protocol. Attends Investigator meetings and conferences as required. Performs other duties as assigned. Education: Required: Associate' Degree in Nursing. Preferred: Bachelor's Degree in Nursing. Experience: Required: 1 year as a Registered Nurse. Licensure/Certification/Listing: Required: Registered Nurse license in North Carolina or a Compact state, Basic Life Support (BLS) or Cardiopulmonary resuscitation (CPR) through American Red Cross or AHA Healthcare Provider.
RN Full-time
Cedars-Sinai

Research Nurse Coordinator II - Biomedical Imaging Research Insititute

Cedars-Sinai Beverly Hills, CA
Job Description The Research Nurse Coordinator II is responsible for all activities associated with clinical study coordination, subject recruitment/enrollment, data management/integrity, regulatory compliance, project/study evaluation and interfacing with participants and family members. Coordinates the clinical logistics of the study, and works in tandem with the Research and/or Clinical Nurse who work to provide hands-on clinical care to research participants. Utilizes clinical nursing background and extensive research protocol knowledge to serve as a liaison between nursing staff, Principal Investigator, other research staff, and study participants. Assists with the education of staff, and provides general oversight of research portfolio as it pertains to the clinical coordination of the studies. Primary Duties and Responsibilities Responsible for clinical study activities, coordination, adherence to protocols and serves as a liaison between study participants, Principal Investigator (PI), and other research staff. Provides educational services to research participants and family regarding study participation, participants current clinical condition, and or disease process. Assesses and documents adverse events as reported by research participants, works closely with PI to document according to department process (grade, attribution, treatment, etc.), and reports to regulatory and sponsor as required. Records research data where assessed or reported by patient (i.e. symptoms of treatment). Creates and presents education materials to the interdisciplinary team on study requirements. Collaborates with the interdisciplinary team to create and communicate a plan of care that allows for safe and effective collection of clinical research data. Triages patient by phone and provides clinical information to the patient. Completes and documents study participant enrollment, assessment/reassessment, education, and follow-up activities and ensures protocol is followed. Coordinates study participant tests and procedures as required. Prepares data spreadsheets for Investigator and/or department. Performs oversight of research portfolio as it pertains to the clinical coordination of the studies. Assists with the education of staff. May assist with grant proposals, publication preparation, and presentations. May process, ship, track or otherwise handle research specimens. Department-Specific Responsibilities: Daily and monthly check of crash cart, temperature logs for refrigerator and drug cabinet. Maintenance and replenishment of expired medical items. Inventory, par levels, and ordering drugs/supplies. Maintaining iSTAT and glucometer QC, software updates, and uploads. Weekly check of emergency call lights, water and patient/volunteer snacks. Research subject transport to and from Taper registration. Research pharmaceutical stress test preparation, to include pre and post 12-lead EKG, lung auscultation, calculation of dose, pump set up, emergency medications, monitoring of vital signs, documentation and charting. Conducting annual mock code blue training. Performing annual N-95 mask fit testing for the RIC. Clinical PET/MR patient transport to and from Taper registration, chart review for MRI safety, allergies, and vital safety details to prevent adverse events. Place IV lines, draw blood, and monitor for contrast reactions. Work with regulatory personnel to ensure compliance for all research studies being performed in the Research Imaging Core. Submission to the medical directors for new project initiation approval, documentation for incidental finding reports and follow up communication. Prepare charts, regulatory forms, perform submission, tracking, enrollment reports, and data entry. Provide, disburse, and track compensation and parking passes to research subjects. Create research charts in Epic for professional research reports, track and send completed reads. Qualifications Education Assoc. Degree/College Diploma Nursing - minimum Bachelor's Degree Nursing or Health Science - preferred Experience 3 years Clinical nursing experience - minimum 2 years Clinical research experience - minimum Licenses and Certifications RN State License - minimum Basic Life Support - minimum
LPN Full-time
Avera Health

Clinical Research Coordinator | Registered Nurse or LPN

Avera Health Sioux Falls, SD
$24.50 - $46.25 / hour
Location: Avera McKennan Hospital Worker Type: Regular Work Shift: Day Shift (United States of America) Pay Range: The pay range for this position is listed below. Actual pay rate dependent upon experience. $24.50 - $46.25 Position Highlights Clinical Research Nurses play a critical role in clinical research studies and the development of new treatments and therapies. They are responsible for daily clinical trial activities including patient screening, recruitment, and enrollment, collecting and managing data, and maintaining compliance with the protocol and regulatory requirements. They will work directly with patients and conduct study assessments, lab draws, EKGs, vital signs, study drug injections, and patient education. They will work with a multidisciplinary team including pharmacy, principal investigators, sponsors, and other parties. Collect and maintain study records and document patient information in an electronic database. *As a Clinical Research Nurse Coordinator, responsibilities & daily activities may include: Reviewing medical records to determine whether interested patients meet inclusion criteria for specific studies. Recruiting potential patients and scheduling patient research visits Documenting information from subject visits and study assessments into an electronic database. Conducting study assessments with study patients including informed consent, lab draws, EKGs, scales, vital signs, and study drug injections. Disburses investigational drug and provides patient teaching regarding administration in collaboration with pharmacists. Process and ship specimen samples including blood and urine per protocol. Collaborate with the research team including pharmacy, principal investigators, sponsors, and external parties. Monitor subject status during treatment and report adverse events and protocol deviations. Maintain accurate and up-to-date study documentation, including informed consent forms, case report forms, and subject binders Ensure study protocols are implemented according to Good Clinical Practice (GCP) guidelines and FDA regulations We are looking to fill two open LPN or RN positions in our team. One position will predominately work on sponsored clinical trials. Our other open LPN or RN coordinator position will predominately support the ECHO study. The ECHO study (Environmental influences on Child Health Outcomes) is a longitudinal, observational study following pregnant women and their children to understand how environmental exposures in the prenatal and early childhood time frame affect health outcomes for children later in life. You Belong at Avera Be part of a multidisciplinary team built with compassion and the goal of Moving Health Forward for you and our patients. Work where you matter. A Brief Overview Provides for the delivery of professional nursing care under the direction of medical providers as related to research study protocols. This position will provide care to patients of all ages involved in clinical trial research studies. This position is an opportunity to learn daily and contribute to research of the future. This position requires close collaboration with the research team to ensure safe and compliant adherence to the research protocol. Enthusiasm for learning is required as is participation in informing participants, physicians, nurses, and other personnel of the research process. What you will do Performs general nursing care to patients which may include observing, recording, and reporting on the patient’s condition, reaction to procedures, and drug accountability. Coordinates research activities with patients of all ages. Records information in electronic medical record and source documents. Greet patients, obtains physical measurements such as height, weight, and blood pressure, medical history information and prepares patient for research related activities. Instructs patients in the collection of samples and tests. Responds to and refers incoming telephone calls. Instructs research patient and family regarding medications and treatment instructions. Documents such information in patient chart. Maintains and reviews patient records to ensure documentation is complete and follow-up has been scheduled and/or completed. Educates patient and family about research study processes, which may include obtaining informed consent. Maintains the exam room by making sure it is clean and adequately stocked with supplies and linen. Prepares list of medical supplies needed. Assists with monitoring and efficiently organizing all research related procedure supplies. Maintains competency of research related processes necessary for properly conducting the research protocol. Works collaboratively with the research team utilizing patient-centered approach with each encounter to provide high quality care, collecting high quality data. Essential Qualifications The individual must be able to work the hours specified. To perform this job successfully, an individual must be able to perform each essential job function satisfactorily including having visual acuity adequate to perform position duties and the ability to communicate effectively with others, hear, understand and distinguish speech and other sounds. These requirements and those listed above are representative of the knowledge, skills, and abilities required to perform the essential job functions. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential job functions, as long as the accommodations do not cause undue hardship to the employer. Required Education, License/Certification, or Work Experience: Registered Nurse (RN) - Board of Nursing An active license in the state of practice Upon Hire Preferred Education, License/Certification, or Work Experience: 1-3 years nursing experience 1-3 years research and/or child development/assessment experience 1-3 years experience interacting with children in a professional setting Expectations and Standards Commitment to the daily application of Avera’s mission, vision, core values, and social principles to serve patients, their families, and our community. Promote Avera’s values of compassion, hospitality, and stewardship. Uphold Avera’s standards of Communication, Attitude, Responsiveness, and Engagement (CARE) with enthusiasm and sincerity. Maintain confidentiality. Work effectively in a team environment, coordinating work flow with other team members and ensuring a productive and efficient environment. Comply with safety principles, laws, regulations, and standards associated with, but not limited to, CMS, The Joint Commission, DHHS, and OSHA if applicable. Benefits You Need & Then Some Avera is proud to offer a wide range of benefits to qualifying part-time and full-time employees. We support you with opportunities to help live balanced, healthy lives. Benefits are designed to meet needs of today and into the future. PTO available day 1 for eligible hires. Up to 5% employer matching contribution for retirement Career development guided by hands-on training and mentorship Avera is an Equal Opportunity Employer - Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, Veteran Status, or other categories protected by law. If you are an individual with a disability and would like to request an accommodation for help with your online application, please call 1-605-504-4444 or send an email to talent@avera.org .
RN Part-time
MyMichigan Health

Clinical Research Nurse RN

MyMichigan Health Midland, MI
Summary Clinical Research Nursing is the specialized practice of professional nursing focused on maintaining equilibrium between care of the research participant and fidelity of the research protocol (ANA, 2016). The Clinical Research Nurse is responsible for human subject protection, care coordination and continuity, contribution to clinical science, clinical practice and study management. (IACRN, 2012). MyMichigan Clinical Research Nurses work within a dedicated Research Department as a part of the health system focused primarily on clinical trials in multiple specialty areas. Clinical trials may include pharmaceutical and device trials and other research projects directly related to patient treatment or care. The Clinical Research Nurse works under the guidance and supervision of the Principal Investigator, ensures the integrity and quality of clinical trials are maintained and conducted with federal, state, and local regulations, IRB board approvals, and MyMichigan Health policies and procedures. Responsibilities (50%)* – Providing Direct Patient Care to Research Study Participants Ensure compliance with each study’s protocol by providing through review and documentation at each study visit Participates in recruitment and selection of study participants by interviewing and documenting medical history to determine compliance with eligibility requirements Performs medical tests, including but not limited to, vital signs, lab draws and processing, and electrocardiograms Administers investigational medication and performs patient assessments during clinic visits to determine presence of side effects; notifies Principal Investigator of findings/issues Provides patient education and medical information to study participants to ensure understanding of proper medication dosage, administration, and disease treatment Documents medical data in patient chart to capture protocol requirements (40%)* As a study coordinator, ensures assigned studies are conducted inaccordance with the Food and Drug Administration (FDA), Office of Research Protections (OHRP ), and Good Clinical Practice (GCP)guidelines Ensure site compliance with research protocols by reviewing all regulatory requirements to confirm implementation of appropriate methods, practices, and procedures for all research activities Develops accurate source materials to ensure compliance from all site staff Provides accurate and timely data collection, documentation, entry, and reporting in both sponsors, Clinical Research leadership, and overseeing IRB, as indicated Ensures appropriate training and credentialing for assigned protocols and associated staff Supports the regulatory staff in the maintenance of regulatory documents Communicates and collaborates specific study requirements to there search team, including internal and external parties, sponsors, monitors, PI, and study participants Ensures compliance with research protocols through participation in ongoing quality control audits, including maintaining ongoing investigational drug accountability (10%)* – Complete required professional development and compliance training activities required by MyMichigan Health and as needed for the position. Maintain Good Clinical Practice, IATA, and other training as required Complete Annual Compliance Modules for position Participate as a part of the research team to identify and prioritize the development of systems and infrastructure to maintain research quality and compliance Occasional travel to attend sponsor study training meetings On-call for weekends/evenings – rotated among all study coordinators – based on FTE allocation Other Duties And Responsibilities Demonstrate excellent customer service. Always promotes subject safety. Contribute to the MyMichigan Health organization targets for patient satisfaction and net operating margin. Follow ALCOA principles for research documentation. Establish effective working relationships with participants, families, physicians, physician office staff, hospital staff, pharmaceutical company representatives, and research related visitors. Acts as liaison between all involved clinical areas and staff of the protocol requirements. Work collaboratively with investigators, sub investigators, referring physicians, other clinical research nurses, and hospital staff. Provides education for patients and families regarding the protocol, including the disease process, plan of care, symptom awareness, and the need to report adverse events. Provide in service education to the clinical staff of the hospitals (pharmacy, nursing, etc.) related to investigational drugs, devices, or procedures, including physiological effects, drug interactions, side effects, nursing care considerations, etc. Communicate serious adverse events to all appropriate sources. Accountable to the Manager of Cardiovascular Research. Represent MyMichigan Health as a professional, high-quality clinical site. Prepares, coordinates, and participates in on-site monitor visits. Analyzes protocol and assists in the creation of source documents. Coordinates activities related to billing, notification of appropriate departments, lab orders, etc. Understand and contribute to the functional unit plan goals and objectives that align with the organization's strategic plan. Follow patients and complete post-hospital follow ups, including clinical assessments. Performs blood draws and basic lab tests as required by the protocol. Coordinates and provides patient care and follow up to research patients as indicated per protocol and remains available 24 hours daily when on call. Educate study participants about their rights as research subjects, answer questions, and refer these to the primary investigator. Ascertain the adequacy of the document and obtain informed consent following the federal regulations before beginning study related procedures. Provides a copy of signed informed consent to the participant. Serve as a resource (along with the PI) for questions or concerns of the participant. Maintain OSHA and Universal Precautions and associated training. Keep participant's welfare uppermost in mind regarding emergencies, study procedures, termination of the study, etc. Provides participants with research-related materials. Reviews and has knowledge of Clinical Research policies and procedures. Complete and maintain source documents. Establishes procedures for randomization, blinding, and data collection. Resolve all sponsor queries regarding participant information. Per standard operating procedures, document follow up with participants about ongoing adverse events after study completion. Maintains, closes, and archives study documents according to standard operating procedure. Certifications and Licensures ACLS - Advanced Cardiac Life Support Preferred BLS - Basic Life Support Required Equivalent Experience - Within 1 month of hire or transfer RN - Registered Nurse Preferred Required Required Equivalent Experience - BSN is preferred. Required Education Education: Associates Degree Comments: Bachelor's degree in nursing preferred. Other Information Experience, Training And Skills Valid RN license Two years of recent clinical nursing experience in a hospital, clinic, or similar health care setting Knowledge of medical terminology, drug calculation skills, clinical medicine, clinical trials, and GCP concepts Knowledge of federal, state and local regulations, including HIPAA policies and procedures Detail oriented and meticulous in all aspects of work Strong follow through skills and ability to proactively identify and solve problems; demonstrated initiative is imperative Must have a professional demeanor, strong communication skills with patients and physicians and co-workers Ability to work independently and as a part of a team Strong interpersonal, customer service, and multi-tasking skills are critical Must be proficient in Microsoft Office Word and EXCEL, electronic health systems and databases used in the research environment, or have the willingness to learn and demonstrate proficiency Ability to work well under pressure, multi-task, and manage deadlines Physical/Mental Requirements And Typical Working Conditions Exposure to stressful situations, including those involving public contact, as well as, trauma, grief and death. Able to wear personal protective equipment that includes latex materials or appropriate substitute if required for your position. Can move freely about facility with or without an assisted device and must be able to perform the functions of the job as outlined in the job description. Overall vision and hearing are necessary with or without assisted device(s). Frequently required to sit/stand/walk for long periods of time. May require frequent postural changes such as stooping, kneeling or crouching. Some exposure to blood borne pathogens and other potentially infectious material. Must follow MyMichigan Health bloodborne pathogen and TB testing as required. Ability to handle multiple tasks, get along with others, work independently, regular and predictable attendance and ability to stay awake. Overall dexterity is required including handling, reaching, grasping, fingering and feeling. May require repetition of these movements on a regular to frequent basis. Physical Demand Level: Medium. Must be able to occasionally (0?33% of the workday) lift or carry 21?50 lbs., frequently 34?66% of the workday 20 lbs. and or Walk/Stand/Push/Pull of Arm/Leg controls and constantly (67?100% or the workday) 10 lbs. Equivalent Experience And Other Comments (Education) Other Comments
RN Full-time
Cincinnati Children's

Research Nurse I/II, Clinical Research Services

Cincinnati Children's Cincinnati, OH
Division of Clinical Research Services Scheduling details: Normal business hours with flexibility (department policy is to not start habitually before 6am or after 10am, anytime in between is fine). Option to work 4 ten-hour days after one year of employment. May be required to travel to other CCHMC locations, but most of our work is done at base. The schedule is flexible and can be flexed based on patient needs (for example, if they have a research visit that lasts 10-12 hours- they can flex their time another day to work less). There is also the option to work remote up to 2 days per week after 6 months of employment. JOB RESPONSIBILITIES Patient/Participant Care- Recognizes and accesses systems and processes within the clinical research environment that affect the research participant experience. Acts as a resource to team members in using these systems and processes. Anticipates needs and responds to subtle changes of research participant and families moving through the research study and healthcare system. Tailors caring practices to individuality of research participant & family providing a healing environment to meet their needs. Promotes safety; demonstrates awareness of potential adverse events' & increases awareness of other team members throughout research study. Assessment- Assess participants, clients and families, whose needs range from uncomplicated to highly complex and quickly recognize normal parameters, deviations and abnormalities in physical, emotional, developmental and behavioral status based on past nursing experience. Develop a plan of care, and effectively prioritize both expected and unanticipated needs for the participants involvement in the research study and make determination of clinical relevance of study procedures and tests. Involve participant, clients, families, and clinical research and health team members in establishing protocol specific research study implementation and adherence goals. Demonstrate proficiency in the implementation of the technical skills. Demonstrate initiative in remaining current on CCHMC policies, standard operating procedures and good clinical and research practices. Demonstrate critical thinking skills by making appropriate nursing decisions, prioritizing both planned and unplanned events for protocol implementation, and proactively addressing potential and actual problems. Implement age appropriate care, including sensitivity to assent and consent in research participation. Compliance- Sustain a working understanding of regulatory requirements and accreditation standards that govern clinical research. Act as a resource to peers. Be mindful and judicious in monitoring safety and departmental policies and procedures. Seeks ways to minimize risk. Organize, oversee and participate with clinical staff in soliciting, enrolling and following participants through clinical studies in accordance with regulatory requirements in a timely and efficient manner. Advocate for research participant to ensure they get the best for their involvement in the study. Educate participants/families on purpose of the research study, study procedures, potential benefits/risks, and rights of research participants during the screening and enrollment process. Ensure informed consent process is carried out correctly and all patient/participant questions and concerns are addressed prior to signing consent form. Research- Guide others in performing procedures, collecting data, analyzing data and making decisions regarding clinical research care, including initial screening, assessment, diagnosis, care, reassessment and modification of care. Intervene for the attainment of research care goals. Ensure proper follow-up of study subjects to ensure compliance, collection of study specimens, and schedule of study visits. Evaluate effectiveness of research care giving, and shows on going follow through in care delivery. Collaborate effectively with investigators to ensure proper progress and completion of clinical studies. Demonstrate proficiency and compliance with established practices in documentation. Maintain records and files required by regulatory agencies and industrial sponsors for clinical studies. Demonstrate awareness of the value and relevance of research and evidence based practice in nursing. Practice can be identified as research based. Process Improvement- Provides a leadership role in developing, implementing and evaluating the conduct of clinical research. Assist peers and team members in acquiring department specific knowledge, skills and behaviors. Contribute to and coordinate discussion in clinical research care conferences, committee meetings, in-services, staff conferences, council activities, seminars and literature. Participate in improving organizational performance through recommending areas or approaches for improvement activities, performing new procedures, collecting data and providing input to department discussions. Motivates and challenges others by displaying energy and enthusiasm in proactively creating a positive work environment. Is self-directed in assuming responsibilities within the team and care delivery system. Assume responsibility for own learning. Initiate activities toward meeting those needs and integrate new knowledge into practice. Participate in establishing job requirements and goals; perform duties at the desired level of competency. Is recognized as a role model and department resource for clinical research and nursing practice, and operational systems. Acts as a preceptor. Guides, nurtures, and contributes to the growth of others by sharing knowledge and skills. Actively participates as a front line example of extraordinary customer service. Contribute to and coordinate discussion in clinical research care conferences, committee meetings, in-services, staff conferences, council activities, seminars and literature. JOB QUALIFICATIONS Bachelor's degree in a related field 2+ years of work experience in a related job discipline Requires clinical license Current Ohio RN license Primary Location Location T Schedule Full time Shift Day (United States of America) Department Clinical Research Services Employee Status Regular FTE 1 Weekly Hours 40 About Us At Cincinnati Children’s, we come to work with one goal: to make children’s health better. We believe in a holistic team approach, both in caring for patients and their families, and in advancing science and discovery. We strive to do better and find energy and inspiration in our shared purpose. If you want to be the best you can be, you can do it at Cincinnati Children’s. Cincinnati Children's is: Recognized by U.S. News & World Report as a top 10 best Children's Hospitals in the nation for more than 15 years Consistently among the top 3 Children's Hospitals for National Institutes of Health (NIH) Funding Recognized as one of America’s Best Large Employers (2025) , America’s Best Employers for New Grads (2025) One of the nation's America’s Most Innovative Companies as noted by Fortune Consistently certified as great place to work A Leading Disability Employer as noted by the National Organization on Disability Magnet® designated for the fourth consecutive time by the American Nurses Credentialing Center (ANCC) We Embrace Innovation—Together. We believe in empowering our teams with the tools that help us work smarter and care better. That’s why we support the responsible use of artificial intelligence. By encouraging innovation, we’re creating space for new ideas, better outcomes, and a stronger future—for all of us. Comprehensive job description provided upon request. Cincinnati Children’s is proud to be an Equal Opportunity Employer committed to creating an environment of dignity and respect for all our employees, patients, and families. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, genetic information, national origin, sexual orientation, gender identity, disability or protected veteran status. EEO/Veteran/Disability
RN Oncology Full-time
Cleveland Clinic

Research Nurse Coordinator - Oncology/Hematology

Cleveland Clinic Weston, FL
At Cleveland Clinic Health System, we believe in a better future for healthcare. And each of us is responsible for honoring our commitment to excellence, pushing the boundaries and transforming the patient experience, every day. We all have the power to help, heal and change lives — beginning with our own. That’s the power of the Cleveland Clinic Health System team, and The Power of Every One. Job Title Research Nurse Coordinator - Oncology/Hematology Location Weston Facility Florida Weston Hospital Department Research-Weston Hospital Job Code 000497 Shift Days Schedule 8:00am-5:00pm Job Summary Job Details Join Cleveland Clinic Weston Hospital’s team of caregivers that remain on the leading edge of technology and education, all while consistently providing patient-centered healthcare. As part of Cleveland Clinic’s Florida region, Weston Hospital is recognized as one of the top hospitals in the Miami-Fort Lauderdale and Florida regions. Here, you will receive endless support and appreciation while building a rewarding career with one of the most respected healthcare organizations in the world. As a Research Nurse Coordinator, you will ensure compliance with research program requirements and associated research studies while coordinating the implementation and conduct of medium to high complexity human subject research projects. In this role, you will serve as a liaison among physicians, sponsors, regulatory agencies, ethics committees, and research staff, coordinating regulatory submissions, IRB communications, study documentation, and credentialing requirements to ensure compliance with FDA, sponsor, and institutional standards. You will have the unique opportunity to help build and develop a growing research program from the ground up while collaborating closely with Main Campus teams. Initially supporting Phase II and III clinical trials, you will help establish processes and infrastructure for an expanding Phase I program. While much of the work is completed behind the scenes, you will play a critical role in advancing research initiatives and, following training, will also support clinical study activities such as research related infusions. A caregiver in this role works days from 8:00 a.m. – 5:00 p.m. (flexible start/end times) After six months, this position offers a hybrid schedule consisting of one remote day and four onsite days each week. A caregiver who excels in this role will: Coordinate the implementation and conduct of research projects, ensuring adherence to research protocol requirements and timely completion. Complete and communicate regulatory documents, develop data and monitoring plans, report Serious Adverse Events as they occur, and complete FDA and sponsor forms. Serve as a liaison between investigators, research personnel, outside study personnel, and central research administration offices to assist in protocol interpretation, enrollment, and safety questions. Assess research subjects, complete nursing assessments, document findings in research subject records, and notify the physician of abnormal findings. Establish a care plan in collaboration with the research subject, family, and research team, and coordinate ongoing care. Identify discharge needs and facilitate discharge planning as appropriate. Perform telephone triage, nursing procedures, and treatments. Evaluate, initiate, and maintain standards of care consistent with CCHS policies and procedures. Assist with specialized patient care equipment as required by the clinical research protocol. Administer medications and treatments as ordered by a physician or licensed independent provider (LIP). Direct, coordinate, and participate in the evaluation and supervision of nursing care provided to research subjects, establishing patient care priorities and delegating nursing activities according to patient needs and staff capabilities. Participate in education, research and performance improvement activities. Develop and maintain knowledge of research protocol to coordinate the comprehensive and compliant execution of assigned protocols. Assist with preparation for audits and response to audits. Maintain professional relationships, including frequent and open effective communication with internal and external constituents. Assist with the development of training and educational material for assigned research protocols. Provide and document education as needed. Conduct and document the informed consent process. Assist with research study design, development of research protocol and research project budget development. Other duties as assigned. Minimum qualifications for the ideal future caregiver include: Graduate from an accredited school of professional nursing Current state licensure as a Registered Nurse (RN) Basic Life Support (BLS) Certification through the American Heart Association (AHA) or American Red Cross Four years of clinical experience Two years of research experience Understanding of the research process and terminology In-depth knowledge of the specialty under investigation Working knowledge of federal regulations and good clinical practice (GCP) Within 90 days of hire, must successfully complete certification in Human Subjects Research as required by the Responsible Conduct of Research guidelines adopted by Cleveland Clinic Preferred qualifications for the ideal future caregiver include: Bachelor’s of Science in Nursing (BSN) Critical care and/or oncology experience Clinical research experience RN experience or knowledge Physical Requirements: Requires full range of body motion, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extended periods of time. Requires corrected vision and hearing to normal range. Requires working under stressful conditions and irregular hours. Exposure to communicable diseases and/or body fluids. Medium Work - Exerting 20 to 50 pounds of force occasionally, and/or 10 to 25 pounds of force frequently, and/or greater than negligible up to 10 pounds of force constantly to move objects. Physical Demand requirements are in excess of those for Light Work. Personal Protective Equipment: Follows standard precautions using personal protective equipment as required. The policy of Cleveland Clinic Health System and its system hospitals (Cleveland Clinic Health System) is to provide equal opportunity to all of our caregivers and applicants for employment in our drug free environment. All offers of employment are followed by testing for controlled substances. Cleveland Clinic Health System administers an influenza prevention program. You will be required to comply with this program, which will include obtaining an influenza vaccination on an annual basis or obtaining an approved exemption. Decisions concerning employment, transfers and promotions are made upon the basis of the best qualified candidate without regard to color, race, religion, national origin, age, sex, sexual orientation, marital status, ancestry, status as a disabled or Vietnam era veteran or any other characteristic protected by law. Information provided on this application may be shared with any Cleveland Clinic Health System facility. If applying for a Florida position, please see the following website for more information on the background screening requirements required by the Agency of Health Care Administration: https://info.flclearinghouse.com/ Please review the Equal Employment Opportunity poster . Cleveland Clinic is pleased to be an equal employment opportunity employer.
RN Full-time
Moffitt Cancer Center

CLINICAL RESEARCH RN I

Moffitt Cancer Center Tampa, FL
Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces. Summary The Clinical Research RN I (CRN I) facilitates clinical research activity at Moffitt Cancer Center and/or affiliated institutions by leading the coordination of opening new protocols, new patient evaluation, registering eligible patients and coordinating protocol‐related care of patients enrolled on clinical trials. The CRN I is required to have an in‐depth knowledge of protocol requirements and good clinical practices as set forth by Federal regulations. As the primary resource for the protocols, the research nurse will coordinate and provide direct patient care, perform ongoing assessments, deliver patient education, and document in accordance with standards and regulatory guidelines pertaining to specified research patients enrolled onto Moffitt run clinical trials. The CRN I will act as liaison between the investigators, primary care providers, Moffitt regulatory staff and the sponsor. Along with the investigator, the CRN I will screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. In addition, this position is responsible for data and source documentation, adverse experience reporting, maintenance of regulatory files in conjunction with the regulatory specialist, maintenance of subject accruals and protocol tracking. The Clinical Research RN I (CRN I) facilitate clinical research activity at Moffitt Cancer Center and/or affiliated institutions by leading the coordination of opening new protocols, new patient evaluation, registering eligible patients and coordinating protocol‐related care of patients enrolled in clinical trials. The CRN I is required to have in‐depth knowledge of protocol requirements and good clinical practices as set forth by Federal regulations. As the primary resource for the protocols, the research nurse will coordinate and provide direct patient care, perform ongoing assessments, deliver patient education, and document in accordance with standards and regulatory guidelines pertaining to specified research patients enrolled into Moffitt run clinical trials. The Clinical Research RN I (CRN) will act as liaison between the investigators, primary care providers, Moffitt regulatory staff and the sponsor. Along with the investigator, the CRN I will screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. In addition, this position is responsible for data and source documentation, adverse experience reporting, maintenance of regulatory files in conjunction with the regulatory specialist, maintenance of subject accruals and protocol tracking. The ideal candidate will have the following qualifications: Direct research nursing experience Ability to plan, organizes, and coordinate multiple work assignments. Ability to establish and maintain effective, collaborative working relationships with others. Ability to clearly communicate verbally and in writing. Ability to establish and maintain effective, collaborative working relationships with others. Credentials and Qualifications: BSN from an ACEN or CCNE accredited institution, no experience required, or ASN from an ACEN or CCNE accredited institution with 2 years of relevant experience. FL RN License An applicant for this position, who will be or is seeking Florida licensure by endorsement, must not have any National Practitioner Data Bank (NPDB) reports, unless the applicant has successfully appealed to have their name removed from the NPDB. An applicant is encouraged to conduct a NPDB Self-Query before proceeding with an employment application: https://www.npdb.hrsa.gov/pract/howToGetStarted.jsp Salary Range Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions. We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce. Moffitt Career Site If you have the vision, passion, and dedication to contribute to our mission, then we have a place for you! Equal Employment Opportunity Moffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence. Reasonable Accommodation Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. Moffitt endeavors to make moffitt.org/careers accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact one of the Human Resources receptionists by phone at 813-745-7899 or by email at HRReceptionists@moffitt.org. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications. Read more information about your EEO rights under the law. Transparency in Coverage Rule
RN Full-time
Moffitt Cancer Center

CLINICAL RESEARCH RN II

Moffitt Cancer Center Tampa, FL
Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces. Summary The Clinical Research Nurse II (CRN II) facilitates clinical research activity at Moffitt Cancer Center and/or affiliated institutions by leading the coordination of opening new protocols, new patient evaluation, registering eligible patients and coordinating protocol-related care of patients enrolled on clinical trials. The CRN II is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by Federal regulations. As the primary resource for the protocols, the CRN II will coordinate and provide direct patient care, perform ongoing assessments, deliver patient education, and document in accordance with standards and regulatory guidelines pertaining to specified research patients enrolled onto Moffitt run clinical trials. The CRN II will act as liaison between the investigators, primary care providers, Moffitt regulatory staff and the sponsor. Along with the investigator, CRN II will screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. In addition, the CRN II is responsible for data and source documentation, adverse experience reporting, maintenance of regulatory files in conjunction with the regulatory specialist, maintenance of subject accruals and protocol tracking Job Summary The Clinical Research Nurse II (CRN II) facilitates clinical research activity at Moffitt Cancer Center and/or affiliated institutions by leading the coordination of opening new protocols, new patient evaluation, registering eligible patients and coordinating protocol-related care of patients enrolled on clinical trials. The CRN II is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by Federal regulations. As the primary resource for the protocols, the CRN II will coordinate and provide direct patient care, perform ongoing assessments, deliver patient education, and document in accordance with standards and regulatory guidelines pertaining to specified research patients enrolled in Moffitt-run clinical trials. The CRN II will act as liaison between the investigators, primary care providers, Moffitt regulatory staff and the sponsor. Along with the investigator, CRN II will screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. In addition, the CRN II is responsible for data and source documentation, adverse experience reporting, maintenance of regulatory files in conjunction with the regulatory specialist, maintenance of subject accruals and protocol tracking. Minimum Experience Required Education: BSN from an ACEN or CCNE accredited institution, with a current FL RN license and three (3) years of relevant nursing experience. Two of the three years of experience must be direct research nursing experience. * in lieu of BSN an ADN/ASN (associate degree in nursing) from an ACEN or CCNE accredited institution with a current Florida RN license with five (5) years of relevant nursing experience. Two of the five years must be direct research nursing experience. An applicant for this position, who will be or is seeking Florida licensure by endorsement, must not have any National Practitioner Data Bank (NPDB) reports, unless the applicant has successfully appealed to have their name removed from the NPDB. An applicant is encouraged to conduct a NPDB Self-Query before proceeding with an employment application: https://www.npdb.hrsa.gov/pract/howToGetStarted.jsp Salary Range Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions. We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce. Moffitt Career Site If you have the vision, passion, and dedication to contribute to our mission, then we have a place for you! Equal Employment Opportunity Moffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence. Reasonable Accommodation Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. Moffitt endeavors to make moffitt.org/careers accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact one of the Human Resources receptionists by phone at 813-745-7899 or by email at HRReceptionists@moffitt.org. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications. Read more information about your EEO rights under the law. Transparency in Coverage Rule
RN Full-time
Texas Health Resources

Clinical Research RN - Full time

Texas Health Resources Fort Worth, TX
26006223 Clinical Research RN Bring your passion to Texas Health so we are Better + Together Work location: Texas Health Fort Worth: 1300 W Terrell Ave, ste K250; Fort Worth, Texas 76104 Work hours: Monday – Friday from 8am – 5pm Department Highlights Strong team with strong, collaborative relationships Works closely with the Cardiovascular Structural Heart team Opportunity to innovate healthcare Here’s What You Need Associate’s Degree in nursing required Bachelor’s degree in nursing preferred 6 months ICU/CCU/ ER experience or equivalent required or 2 years conducting clinical research (drug, devices, etc) required Clinical Research experience preferred Research training via CITI (Human subject Protection and Good Clinical Practice) preferred Epic EMR, Realtime CTMS and SharePoint experience preferred Dangerous Shipping Goods/Materials Certificate preferred RN upon hire required ACLS upon hire preferred CPR within 30 days of hire and maintained every 2 years What You Will Do Conduct clinical studies according to FDA, CFR and ICH regulations and guidelines: from pre-study to startup to closeout. Including: Study Startup: coordination and facilitation of all departments and various organizations to successfully startup a study from feasibility to first Be knowledgeable of the Sponsor’s protocol so that all study activities are completed correctly and completely. Train other site personnel, and medical staff, on the specifics of implementing assigned protocols; including the regulations and expectations of monitors. Educate participants, families and caregivers regarding protocol requirements and relationship to disease process. Communicate and meet with the Sponsors, IRBs, Physicians, regulatory bodies, etc. regarding essential study activities as necessary, such as the conduct of the study and review study data. Promote and represent the CRD in a positive manner Develop and implement recruitment strategies for studies; which include screening potential study subjects according to the protocol’s inclusion and exclusion criteria. Be available to register participants after hours (on call 24 hours a day and on weekends). Schedule study subjects’ visits and during the study subject’s visit perform defined activities of the study completely and accurately. Complete the CRFs for the study accurately, completely, and in a timely fashion. Maintain adequate and accurate case histories for each study subject and record all observations in the source document during the study. Complete the adverse events source documentation for the sponsor and IRB for review by the Investigator. Including: Design and maintain organizational tools to conduct studies accurately and in compliance with GCP and ICH guidelines. Ensure the safety and welfare of the study subjects. Obtain proper written information consent from each study subject prior to participate in the study Maintain all information in original records and certified copies of original records of clinical findings, observations, or other activities in a clinical trial necessary for the reconstruction and evaluation of the trial. Source data are contained in source documents (original records or certified copies) (ICH 1.51). Unless original copies are required to be kept by the Sponsor (i.e. EKG tracings, patient diaries, questionnaires, etc), then a note to file is placed in the study regulatory binder. Follows electronic source guidelines and certification and destruction of hard copies, when applicable. Including: Assign study subject numbers and maintain accurate and complete records of the receipt, administration, and return of all clinical supplies (including study drug). Assist in maintaining all required documentation in the study regulatory documentation file. Including processing and completing all IRB documentation. Including but not limited to: initial application, Informed Consent, modifications, amendments, Serious Adverse Events, advertisement, etc. Obtain and maintain certification through appropriate accrediting bodies: (RN, and BLS) As well as certification and training required for studies: GCP, HSP, etc Additional perks of being a Texas Health Clinical Research RN Benefits include 401k, PTO, medical, dental, Paid Parental Leave, flex spending, tuition reimbursement, student Loan forgiveness as well as several other benefits. Delivery of high quality of patient care through nursing education, nursing research and innovations in nursing practice. Strong Unit Based Council (UBC). A supportive, team environment with outstanding opportunities for growth. Learn more about our culture, benefits, and recent awards. Do you still have questions or concerns? Feel free to email your questions to recruitment@texashealth.org.
RN Internship
Main Line Health

Clinical Research Nurse I

Main Line Health Bryn Mawr, PA
Could you be our next Clinical Research Nurse I at Lankenau Medical Center/ LIMR? Why work as a Clinical Research Nurse 1 at Main Line Health? Make an Impact! The Clinical Research Nurse I will manage and oversee the day-to-day activities of Phase I-IV clinical research studies, industry trials and grant supported research in accordance with Good Clinical Practice (GCP). Daily tasks may include performing basic nursing skills, study coordination with a central focus on managing subject recruitment and enrollment, consistency of study implementation, data management and integrity, and compliance with regulatory requirements and reporting. The Clinical Research Nurse I coordinates procedures, tests and follow-up visits according to the protocol, provides education to research subjects and staff regarding the investigational study, and promotes patient safety for all research related activities working collaboratively with the physician investigators and a multi-disciplinary team. Join the Team! Like our patients, the Main Line Health Family encompasses a wide range of backgrounds and abilities. Just as each of our patients requires a personalized care plan, each of our employees, physicians, and volunteers, bring distinctive talents to Main Line Health. Regardless of our unique design, we all share a purpose: providing superior service and care. Position-Specific Benefits Include This position is eligible for up to 160 hours of paid time off per year. We also offer a number of employee discounts to various activities, services, and vendors... And employee parking is always free! Position Clinical Research Nurse 1- Oncology experience preferred. Shift Day Shift- 40 hours/week Monday-Friday 8am-4:30pm Experience 0-2 years nursing experience. Clinical research and/or nursing research experience preferred. Clinical research conducted while in the student environment may be considered on a case-by-case basis. Leadership experience in research or healthcare/health care setting preferred Education A current PA RN license if primary state of residence in PA; if live out of PA, a multi-state license verified in one of the approved states through the Nursing Licensure Compact (effective 9/5/23).
RN Full-time
Guthrie

Registered Nurse - Clinical Research - Full Time Day

Guthrie Binghamton, NY
Up To $25,000 Sign On Bonus For Qualified RNs! Position Summary: Coordinate multiple in- patient and out- patient clinical research protocols. This coordination requires extensive knowledge for the disease pathophysiology, pharmacology treatments, patient disease evaluation workflow, and the ability to collaborate and communicate new processes related to research with the involved departments. Education, License & Cert: Must have a Registered Nursing license in PA or NY and meet one of the following: 1. Five years clinical experience in a healthcare setting, or 2. Bachelor of Science degree with 3 years full time nursing experience or 3. Certification as a Clinical Research professional Experience: Desire certification in the disease specialty being studied or as a Clinical Research Professional. Three years full time experience in the nursing field required. Experience successfully leading or advancing a project with peers, leadership, and/or external customers. Essential Functions: Coordinate individual clinical research projects in multiple disease conditions. Project coordination requires meeting sponsor specific training requirements prior to initiation, assuring team members have met sponsor training, training team members to delegated duties, supporting regulatory specialist with sponsor communications, maintaining study supply inventory, and supporting monitors during visits. Each project requires institutional process development strategies. This research team member develops or advances the investigators plans. Collaborate with the manager and executive director for the development of department research programs. This is demonstrated through advancing research meetings in the Guthrie Medical Group departments. These meetings communicate the performance metrics regarding enrollments, training requirements and new protocol opportunities. Additional responsibilities for specific program development include assisting with feasibility, site selection, IRB document review, and corresponding with investigators, IRB, and sponsors. This role coordinates the study protocol procedure events and treatment planning with the investigator. This coordination for the patient includes reviewing medical history for eligibility, educating the patient to the study requirements, registering the participant to the project, and organizing patient visits. Patient visits requirements involve scheduling, reviewing treatment plans, assuring study treatment and supplies are available and documenting the encounter. This documentation must meet Good Clinical Practice standards of attributable, legible, contemporaneous, original, accurate, and complete. Lastly follow- up with the participant related to next visit and study requirements. Administering and dispensing investigational medication ordered for that patient by a licensed physician in the dosage prescribed by protocol. Retrieval of medication and assessment of compliance by patient to the protocol. Other Duties: Routine travel between Guthrie research sites may be required, as well as periodic travel for protocol training. Collaborate with director, manager, research team members and IRB coordinator in developing and revising process flow for research procedures. Attend training seminars and conferences as required by sponsor of research study. Make presentations of study information to groups of physicians and patients. Assist physicians in protocol development. Advise department manager on resource utilization and training needs. Perform other duties as assigned by the director or manager.
RN Full-time
Guthrie

Registered Nurse - Clinical Research - Full Time Day

Guthrie Cortland, NY
Up To $25,000 Sign On Bonus For Qualified RNs! Position Summary: Coordinate multiple in- patient and out- patient clinical research protocols. This coordination requires extensive knowledge for the disease pathophysiology, pharmacology treatments, patient disease evaluation workflow, and the ability to collaborate and communicate new processes related to research with the involved departments. Education, License & Cert: Must have a Registered Nursing license in PA or NY and meet one of the following: 1. Five years clinical experience in a healthcare setting, or 2. Bachelor of Science degree with 3 years full time nursing experience or 3. Certification as a Clinical Research professional Experience: Desire certification in the disease specialty being studied or as a Clinical Research Professional. Three years full time experience in the nursing field required. Experience successfully leading or advancing a project with peers, leadership, and/or external customers. Essential Functions: Coordinate individual clinical research projects in multiple disease conditions. Project coordination requires meeting sponsor specific training requirements prior to initiation, assuring team members have met sponsor training, training team members to delegated duties, supporting regulatory specialist with sponsor communications, maintaining study supply inventory, and supporting monitors during visits. Each project requires institutional process development strategies. This research team member develops or advances the investigators plans. Collaborate with the manager and executive director for the development of department research programs. This is demonstrated through advancing research meetings in the Guthrie Medical Group departments. These meetings communicate the performance metrics regarding enrollments, training requirements and new protocol opportunities. Additional responsibilities for specific program development include assisting with feasibility, site selection, IRB document review, and corresponding with investigators, IRB, and sponsors. This role coordinates the study protocol procedure events and treatment planning with the investigator. This coordination for the patient includes reviewing medical history for eligibility, educating the patient to the study requirements, registering the participant to the project, and organizing patient visits. Patient visits requirements involve scheduling, reviewing treatment plans, assuring study treatment and supplies are available and documenting the encounter. This documentation must meet Good Clinical Practice standards of attributable, legible, contemporaneous, original, accurate, and complete. Lastly follow- up with the participant related to next visit and study requirements. Administering and dispensing investigational medication ordered for that patient by a licensed physician in the dosage prescribed by protocol. Retrieval of medication and assessment of compliance by patient to the protocol. Other Duties: Routine travel between Guthrie research sites may be required, as well as periodic travel for protocol training. Collaborate with director, manager, research team members and IRB coordinator in developing and revising process flow for research procedures. Attend training seminars and conferences as required by sponsor of research study. Make presentations of study information to groups of physicians and patients. Assist physicians in protocol development. Advise department manager on resource utilization and training needs. Perform other duties as assigned by the director or manager.