Diabetes Clinical Research Coordinator (Associate)

Michigan Medicine; Ann Arbor (MI); On-site; USD 60,000 - 90,000; Full time

Job summary

Michigan Medicine in Ann Arbor is seeking a Clinical Research Coordinator Associate to support diabetes-focused studies within the Division of Metabolism, Endocrinology, and Diabetes (MEND). You will coordinate multiple studies, recruit participants, manage data, and ensure protocol compliance under supervision.

The role requires a Bachelor's Degree in Health Science, certification eligibility with ACRP or SOCRA within six months, and at least 2 years of clinical research experience.

Qualifications

• Bachelor's Degree in Health Science or equivalent in combined education and clinical research experience.
• Certification is required through ACRP as a Certified Clinical Research Coordinator or SOCRA as a Certified Clinical Research Professional or equivalent, eligible to register or take exam within six months of hire.
• Minimum 2 years of directly related experience in clinical research and clinical trials.

Responsibilities

• Develop and maintain understanding of study concepts, including research design and diabetes.
• Recruit research participants.
• Conduct participant outreach and communication.
• Schedule participant visits and complete follow-up activities.
• Collect data, including through verbally administered surveys.
• Enter and upload data and perform quality assurance checks.
• Complete study-related documentation.
• Communicate effectively with the study team, including attending weekly team meetings.
• Perform participant safety-related responsibilities, including reporting adverse events and other occurrences.

Skills

Digital proficiency

Communication skills

Quality assurance

Education

Bachelor's Degree in Health Science

ACRP/SOCRA certification eligibility

Job description

Michigan Medicine in Ann Arbor is seeking a Clinical Research Coordinator Associate to support diabetes-focused studies within the Division of Metabolism, Endocrinology, and Diabetes (MEND). You will coordinate multiple studies, recruit participants, manage data, and ensure protocol compliance under supervision.

The role requires a Bachelor's Degree in Health Science, certification eligibility with ACRP or SOCRA within six months, and at least 2 years of clinical research experience.