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How to Apply

A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.

Job Summary

As part of the strategic research initiative, Fast Forward Clinical Trials is engaging the entire UMHS in creating a new model to improve clinical care, value, and health outcomes by successfully executing a diverse portfolio of high-quality clinical trials. This new model entails an organizational structure of local service units, central infrastructure, and governance oversight.  These units will provide a professional environment of expert personnel accessible to all investigators, especially early-career faculty. The entire system is governed by the Medical School Office of Research in partnership with the Clinical Trials Subcommittee of the Research Board of Directors.

In collaboration with the Ambulatory & Chronic Disease Clinical Trials Support Unit Medical Directors, Administrator, and Clinical Research Project Manager, the Clinical Research Coordinator (CRC) will provide a value added service assisting faculty with study coordination of any clinical trials within the CTSU as needed.  This position will be part of a study coordinator pool providing support to all levels of faculty and study teams for clinical trials in the CTSU.  The CRC will be available to assist study teams with study coordinator activities such as screening, consenting and enrolling subjects, collecting and managing patient and laboratory data, data entry, IRB application preparation, and regulatory management.  Additionally, the CRC will manage audits and monitor visits, as well as other duties as needed.  This position could include travel to off-site locations.


Assist study teams with aspects of clinical trial coordination including:  identifying potential subjects, screening subjects, consenting and enrolling subjects, and collecting and managing patient and laboratory data for clinical research subjects. 

Collect specimens and monitor study subjects.  Assist in monitoring of test results.  Ensure integrity of specimens (collection, processing, shipping/packing, storing, labeling, tracking, etc.). 

Perform data management and results reporting, such as entering information into Case Report Forms (CRFs).  Assist with collection of external medical records for study reporting purposes.  Ability to identify and report Adverse Events (AEs) and Serious Adverse Events (SAEs).

Prepare IRB submissions including the initial applications, as well as amendments and scheduled continuing reviews, progress reports, safety reports, and adverse event reports.  

In coordination with other CTSU staff, communicate with sponsor’s concerning progress of clinical trials, billing calendar/budget issues, subject related problems, recruitment strategies, and specific policies and procedures.

Act as liaison between study team and sponsors, IRB, federal, state, and university officials and other regulatory agencies to maintain accurate communication of costs, policy changes, fiscal requirements, and other regulatory issues.  Serve as key resource to research participants and collaborators.  Provide support for audits and monitor visits.

Support other clinical research staff in the ACD CTSU during periods of time where there is an increase in workload or for covering extended absences.   

Work collaboratively with the CTSU team by maintaining a good rapport and communication with research teams and faculty, as well as patients and families.

Staff members are expected to work well in a team setting, but also independently when appropriate and regularly exercise good judgment in setting priorities, resolving operational problems, and applying policies, procedures, and methods, while maintaining the strictest of confidentiality at all times.

Required Qualifications*

  • Bachelor’s degree in a science or health-related field, or equivalent education and experience.
  • Minimum of 3 years of experience as a study coordinator.   (0-1 years of experience for the underfill role)
  • ACRP/SoCRA certification, or effort towards certification.
  • Experience with the IRB application process.
  • Proficient in sample collection/handling.
  • Demonstrated understanding of clinical research; understand compliance issues related to human subjects research, knowledge and application of the Code of Federal Regulations (CFR), Good Clinical Practice (GCP), and FDA regulations.
  • Demonstrated understanding of some medical terminology is required.
  • Excellent interpersonal, oral, and written communication skills with exceptional attention to detail.
  • Proficient computer skills including Microsoft software applications.
  • Ability to organize and manage multiple tasks simultaneously, as well as prioritize and exercise good judgment.
  • Ability to work independently with minimal supervision and with diverse teams of people in a diplomatic, collaborative and effective manner.


Desired Qualifications*

  • Knowledge of UMHS policies and practice.Familiarity with Epic, Mi-Chart and eResearch applications.
  • Familiarity with Epic, Mi-Chart and eResearch applications.
  • PEERS, CITI or NIH Protection of Human Subjects Training Certification.

Work Schedule

Primarily M-F days, however variability will be required by some projects including early mornings, evenings and occasional travel.

Underfill Statement

This position may be underfilled at a lower classification depending on the qualifications of the selected candidate.

Additional Information

Administrative supervision is received from the CTSU Clinical Research Project Manager.  Functional supervision is received from principal investigators.  This position will work in collaboration with other study team members, which may include study coordinators outside of the CTSU.

Background Screening

Michigan Medicine conducts background screening and pre-employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings.  Background screenings are performed in compliance with the Fair Credit Report Act.

Mission Statement

Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally.  Our mission is guided by our Strategic Principles and has three critical components; patient care, education and research that together enhance our contribution to society.

Application Deadline

Job openings are posted for a minimum of seven calendar days. This job may be removed from posting boards and filled anytime after the minimum posting period has ended.

U-M EEO/AA Statement

The University of Michigan is an equal opportunity/affirmative action employer.