Hybrid Clinical Research Technician | Study Coordination & Data

Kappaalphapsi1911; Ann Arbor, Northern (MI, KY); Hybrid; USD 42,000 - 62,000; Full time

Job summary

The University of Michigan is seeking a Clinical Research Technician/Clinical Research Assistant for a term-limited on-site role in Ann Arbor. You will support multiple research projects within the Chronic Pain and Fatigue Research Center, helping with coordination, data entry, and regulatory tasks under supervision.

You will work with a multidisciplinary team, manage participant interactions, and assist with regulatory documents, IRB submissions, and study reporting while upholding strict

Qualifications

• Associate degree in Health Science or equivalent is necessary.
• Minimum 1 year of directly related clinical research experience.
• Advanced degree in health-related fields is acceptable.
• Minimum 3 years of human subject experience (clinical, lab or health regulations) is acceptable.

Responsibilities

• Provide support to participants around technological components of studies, including app installation and electronic consenting.
• Organize outreach to recruitment lists and screen, consent, and enroll participants per protocol.
• Track and follow participants, enter and manage data, and conduct chart reviews as needed.
• Prepare and send participant mailings and support incentives distribution.

Skills

Microsoft Office

Organizational skills

Attention to detail

Data confidentiality

Independent work

Teamwork

Record-keeping

Education

Associate degree in Health Science

Advanced degree in Health Sciences

Minimum 1 year clinical research experience

Bachelor's degree in Health Science

Minimum 3 years of human subject experience

Tools

OnCore

Epic

MiCHART

REDCap

Qualtrics

MyDataHelps

eResearch applications

Job description

The University of Michigan is seeking a Clinical Research Technician/Clinical Research Assistant for a term-limited on-site role in Ann Arbor. You will support multiple research projects within the Chronic Pain and Fatigue Research Center, helping with coordination, data entry, and regulatory tasks under supervision.

You will work with a multidisciplinary team, manage participant interactions, and assist with regulatory documents, IRB submissions, and study reporting while upholding strict