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Clinical Research Rn Jobs in Michigan (NOW HIRING)

Georgetown University

Clinical Research Nurse

Detroit, MI · On-site

$54.62 - $100.49/hr

Job Overview The Clinical Research nurse, Lombardi Cancer Center - Georgetown University, is a ... Valid RN license * Bachelor of Nursing degree * Two (2) years of recent clinical nursing experience ...

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How much do clinical research rn jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical research rn in Michigan is $38.47, according to ZipRecruiter salary data. Most workers in this role earn between $31.63 and $45.67 per hour, depending on experience, location, and employer.

What is a clinical research RN?

Clinical Research Registered Nurses (Clinical Research RNs) are licensed nurses who specialize in conducting and coordinating clinical trials and research studies involving human participants. They collaborate with physicians, researchers, and study coordinators to ensure that research protocols are followed, participants are cared for safely, and all regulatory and ethical guidelines are met. Their duties include administering study medications, collecting data, monitoring patient responses, and educating participants about the study. Clinical Research RNs play a vital role in advancing medical knowledge and improving patient care through research.

How does a clinical research RN typically collaborate with other members of the research team?

A Clinical Research RN works closely with principal investigators, study coordinators, physicians, and data managers to ensure research protocols are followed accurately and patient safety is maintained. They are responsible for communicating patient progress, reporting adverse events, and coordinating care between departments. Regular team meetings and detailed documentation are essential to keep everyone informed and maintain compliance with regulatory standards. This collaborative environment helps ensure research studies run smoothly and efficiently.

What are the key skills and qualifications needed to thrive as a clinical research RN, and why are they important?

To thrive as a Clinical Research RN, you need a solid background in nursing, clinical trial protocols, and regulatory compliance, typically requiring an RN license and experience in research settings. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is often expected. Excellent organizational, communication, and critical thinking skills help you coordinate studies, interact with participants, and collaborate with multidisciplinary teams. These competencies ensure the integrity of research data, patient safety, and successful execution of clinical trials.

What is the difference between Clinical Research Rn vs Clinical Research Coordinator?

AspectClinical Research RnClinical Research Coordinator
CredentialsRN license, possibly specialized certificationsTypically bachelor's degree, certifications like CCRP beneficial
Work EnvironmentHospitals, clinics, research institutionsResearch sites, hospitals, clinics
Job FocusPatient care, protocol adherence, data collectionStudy coordination, participant recruitment, data management

While both roles are involved in clinical research, the Clinical Research Rn primarily provides patient care and ensures protocol compliance from a nursing perspective. The Clinical Research Coordinator manages study logistics, participant recruitment, and data collection. Both roles require strong organizational skills, but the RN's focus is more on patient interaction, whereas the Coordinator handles study operations.

How to get into clinical research as a registered nurse?

To become a clinical research RN, obtain a valid nursing license and gain experience in patient care. Additional certifications such as Certified Clinical Research Professional (CCRP) or Good Clinical Practice (GCP) training can improve job prospects, and familiarity with research protocols and data management is beneficial.

What do clinical research RNs do in clinical research?

Clinical research RNs coordinate and monitor clinical trials by recruiting participants, collecting data, administering treatments, and ensuring compliance with study protocols and regulations. They often work closely with investigators, maintain accurate documentation, and may require certification such as CCRP. Their role is essential for the safe and effective conduct of research studies.

What are popular job titles related to Clinical Research Rn jobs in Michigan?

For Clinical Research Rn jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Clinical Research Rn jobs in Michigan look for?

The top searched job categories for Clinical Research Rn jobs in Michigan are:

Clinical Research Rn jobs near you
Infographic showing various Clinical Research Rn job openings in Michigan as of August 2026, with employment types broken down into 2% As Needed, 70% Full Time, 22% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $80,010 per year, or $38.5 per hour.

Clinical Research RN - Clinical Research RN *Days ( M-F, 8a-5p ) - 40hrs/wk

UM Health-West

Wyoming, MI • On-site

Other

This job post has expired 2 days ago. Applications are no longer accepted.

Job description

Clinical Research RN

Under the supervision of the Director of Clinical Research, the Clinical Research Nurse supports clinical research studies conducted by principal investigator(s) at Metro Health. Coordinates and participates in a variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data to include obtaining trials, screening and consenting of patients, performing patient study-visits, education, data management, and drug/device accountability. Coordinate and perform study specific regulatory processes across multiple studies of different therapeutic areas and phases, in accordance to appropriate regulations, Standard Operating Procedures (SOPS) and study specific protocols.

Requirements:

  • State of MI RN License required
  • Bachelor Degree Required
  • Bachelor degree required. Previous clinical research experience helpful. Bilingual (Spanish) helpful.
  • Must be highly organized and able to multitask.
  • Interact effectively and pleasantly with a diverse population.
  • Ability to review detailed data and make prompt judgments based on that data.
  • Ability to work efficiently and effectively under tight deadlines, interruptions and high work volume.
  • Excellent written and verbal communication skills.
  • Working knowledge of computer and their applications to the related field.
  • Ability to work independently as well as with a team.

Essential Functions and Responsibilities:

  • Coordinate and participate in clinical research studies conducted by principal investigator(s). Coordinate and participate in a variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data. Coordinate and implement procedures to collect data from patient medical records, interviews, questionnaires, diagnostic tests and other sources; code, evaluate and interpret collected data and prepare appropriate documentation; obtain blood samples, cultures, tissues and other specimens for laboratory analysis. Monitor patient's progress to include documentation and reporting of adverse events and unanticipated problems.
  • Perform protocol-required clinical assessments and procedures within State of Michigan Registered Nurse scope of practice and per delegation of the principal investigator..
  • Evaluate and interpret collected clinical data in conjunction with principal investigator(s) as appropriate; prepare oral presentations or written reports and collaborate on the preparation of manuscripts for publication. Review journals, abstracts and scientific literature to keep abreast of new developments and to obtain information regarding previous studies to aid in the planning of new studies.
  • Adhere to study protocol guidelines, Clinical Trial Agreements, and budgets. Ensure compliance with SOPs, FDA (U.S. Food and Drug Administration), NIH (National Institutes of Health) and other applicable regulations. Develop appropriate regulatory reports and associated documentation.
  • Maintain primary responsibility of a variety of regulatory tasks including: assess, complete and submit protocol related documents to the appropriate committees and Institutional Review Board. Maintain essential regulatory documents (to include current CVs, licenses, site laboratory certifications). Coordinate Human Research Subject Training for personnel. Maintain database and system for patient enrollment data, patient files, statistical data and other information pertinent to studies.
  • Perform quality assurance review of study and regulatory documents, submit findings and recommendations in writing. Participate in the audit process by preparing patients records and follow up as necessary. Participate in ongoing process improvement activities, make improvements in data management, and suggest programmatic improvements.
  • Function as resource to others involved in planning, implementation and evaluation of clinical studies. Assist in training new personnel.
  • Communicate and interact with peers and other departments in a manner that is viewed as having a positive effect on patient services. Interact effectively with patients/family members and demonstrate sensitivity in regards to cultural diversity, age specific needs and confidentiality.

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