Clinical Research Technician​/Clinical Research Assistant - Term Limited

# Clinical Research Technician/Clinical Research Assistant - Term Limited University of Michigan Ann Arbor, MIFull-Time Sep 22, 2026

Science##

Job Description ##

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.## 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.##

Job Summary 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.

The Chronic Pain and Fatigue Research Center (CPFRC), located within the Department of Anesthesiology is a collaborative, collegial, and fast paced program that enjoys the opportunity to partner with many researchers from the Schools of Medicine and Public Health, as well as extramural biomedical researchers.  The successful candidate for this position will participate in many aspects of research analysis and collaborative activities, with research programs including longitudinal cohorts, cross-sectional studies, clinical trials, health services and translational research with funding from a variety of sponsors including, NIH, industry, and others.

The CPFRC provides rich opportunities for career development and continued learning from experienced colleagues. The research team includes physicians, biostatisticians, project managers, study coordinators, data managers, and administrative support.

The Clinical Study Coordinator-Technician is expected to work as part of a collaborative team and is responsible for managing their assigned tasks. They are expected to understand and support the conduct of research within all federal, state, and local regulatory requirements. This position provides administrative and coordination support for multiple projects in the conduct of clinical research projects. Assignments may include tasks for both single-center and multi-center studies.

This position may independently provide study coordination for simple and moderately complex clinical research studies.  As a member of a coordination team, this position will help support a portfolio of projects with varying levels of complexity.## Responsibilities
*** Characteristic

Duties and Responsibilities:

** Knowledge of all 8 competency domains is expected:
1. Scientific Concepts and Research Design
2. Ethical Participant Safety Considerations
3. Investigational Products Development and Regulation
4. Clinical Study Operations (GCPs)5. Study and Site Management
6. Data Management and Informatics
7. Leadership and Professionalism
8. Communication and Teamwork
* Provide support to participants around the multiple technological components of research studies and trials, including installing the study smartphone application(s), electronic consenting, and setup of wearable devices, as well as navigating online electronic data capture systems.
* CRC-tech will work with other team members to:  + organize and reach out to lists of participants that may be contacted for recruitment,  + Screen, informed consent, and enrollment of participants according to protocol for research studies,  + track and follow participants in study after their initial enrollment,  + enter and manage data,  + conduct chart reviews as necessary,  + prepare and send participant mailings,  + support the distribution of participant incentives,  + provide customer support around participant usage of the studies?

technologies  + perform other routine project tasks.
* Assist with maintaining regulatory documents and assisting with IRB submissions such as amendments, SAEs and ORIOs.
* May assist in the preparation of a variety of reports such as quarterly updates and regulatory.
* Help build and maintain participant databases for remote data collection and participant scheduling, tracking, and monitoring, including resolving data queries
* Attend…