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Job Summary

The Division of Gastroenterology and Hepatology has an immediate need for a full time Clinical Subjects Coordinator to oversee one newly initiated observational study and one recently initiated clinical trial in the area of liver cirrhosis. The role will involve cognitive testing, speech assessment, and biospecimen collection and analysis, among other research maintenance activities. The coordinator will be supervised by one PI and work with a team of other study coordinators. Studies are sponsored by the University, a GI society, and an industry sponsor.

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.

Why Join Michigan Medicine?

Michigan Medicine is one of the largest health care complexes in the world and has been the site of many groundbreaking medical and technological advancements since the opening of the U-M Medical School in 1850. Michigan Medicine is comprised of over 30,000 employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world’s most distinguished academic health systems.  In some way, great or small, every person here helps to advance this world-class institution. Work at Michigan Medicine and become a victor for the greater good.

What Benefits can you Look Forward to?

  • Excellent medical, dental and vision coverage effective on your very first day
  •  Retirement Savings Opportunities


  • Consent and recruit patients in clinic, by phone, and by email
  • Administer survey questionnaires as well as assessments of speech and cognitive function
  • Coordinate each patient’s study participation from enrollment to completion
  • Liaise with other research groups both at U-M and beyond to ensure seamless study progress
  • Contribute to the design and maintenance of databases, along with routine data entry into those databases and various spreadsheets
  • Analyze cross-sectional and longitudinal study data at various points throughout the study
  • Submit IRB applications, prepare IRB documents, and provide continuing reviews
  • Supervise research students who will assist with clerical data and subject recruitment
  • Management of biospecimens

Required Qualifications*

Bachelor's degree and two years of experience in clinical research including patient recruitment, data management, and IRB applications is necessary.

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. Pre-employment drug testing applies to all selected candidates, including new or additional faculty and staff appointments, as well as transfers from other U-M campuses.

Application Deadline

Job openings are posted for a minimum of seven calendar days.  The review and selection process may begin as early as the eighth day after posting. This opening 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.