Remote-Eligible Clinical Research Coordinator

University Of Michigan

Ann Arbor (MI)

On-site

USD 65,000 - 90,000

Full time

30 hours ago
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Job summary

University of Michigan is seeking an Intermediate Level Clinical Research Coordinator (with option to underfill at Associate level) to lead and support participant recruitment, study visits, remote monitoring, and regulatory compliance across clinical protocols.

This on-site role requires collaboration with clinicians and the PI, adherence to GCP and FDA guidelines, and strong organizational skills to keep data complete and study materials audit-ready.

Qualifications

  • Bachelor's degree in health sciences, biology, nursing, public health, or related field (or equivalent credentials)

Responsibilities

  • Review, comprehend, and execute study protocols and timelines.
  • Coordinate clinical visit activities incl. intake, biospecimen handling, and testing.
  • Ensure all visit activities and source data are complete, accurate, and documented on time.
  • Interact with the study team to ensure participant safety and protocol compliance.
  • Develop recruitment workflows within UM healthcare sites; screen and engage potential participants.
  • Present study details, answer questions, and obtain informed consent.
  • Maintain regulatory binders and audit-ready documentation per GCP/FDA guidelines.
  • Coordinate inter-departmental study requirements to ensure timely processing.

Skills

Interpersonal skills
Organizational skills
Attention to detail
Initiative / Self-starter
Communication with participants
GCP knowledge

Education

Bachelor's degree in health sciences, biology, nursing, public health, or related field

Job description

University of Michigan is seeking an Intermediate Level Clinical Research Coordinator (with option to underfill at Associate level) to lead and support participant recruitment, study visits, remote monitoring, and regulatory compliance across clinical protocols.

This on-site role requires collaboration with clinicians and the PI, adherence to GCP and FDA guidelines, and strong organizational skills to keep data complete and study materials audit-ready.

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