Research Technician Intermediate
Listed on 2026-09-06
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Research/Development
Clinical Research, Research Assistant/Associate -
Healthcare
Clinical Research
Clinical Research Intern
The Michigan Clinical Trial Support Unit Clinical Research Coordinator Unit (M-CTSU CRC Unit) is seeking a part-time Clinical Research Intern to support clinical research activities while gaining structured, hands-on experience in research coordination.
This paid, term-limited position is designed for an individual interested in developing a deeper understanding of clinical research processes, including regulatory compliance, research documentation, participant-facing activities, data management, and research ethics. The selected candidate will work under the guidance of experienced clinical research professionals and receive training, mentorship, and regular feedback throughout the appointment.
The position will provide moderately complex technical and administrative support for clinical research projects. The anticipated appointment is approximately 20 hours per week from September 2026 through May 2027.
The University of Michigan offers a collaborative environment in which employees can contribute to research that advances health and improves patient care. In this position, you will have opportunities to:
- Gain practical experience with clinical research operations
- Learn about institutional, federal, and study-specific research requirements
- Work alongside experienced clinical research coordinators and other research professionals
- Participate in structured training, professional-development activities, and regular mentorship
- Build skills in research documentation, data management, communication, organization, and ethical decision-making
- Learn about career paths in clinical research, medicine, and related health professions
The M-CTSU Clinical Research Intern will work under the direct guidance of experienced clinical research staff and will assist team members who hold delegated study responsibilities. The intern will not independently manage studies, perform project-specific responsibilities, or make decisions regarding participant eligibility, informed consent, protocol implementation, or regulatory compliance.
Responsibilities may include:
- Attend and actively contribute to the unit’s weekly education and training events, including discussions, presentations, workshops, and other professional-development activities.
- Assist delegated study-team members with research documentation, regulatory materials, data collection and entry, data-quality review, and maintenance of study files.
- Observe and support approved participant recruitment, scheduling, study visits, and follow-up activities under appropriate supervision.
- Conduct literature searches and help organize or summarize information relevant to ongoing research projects.
- Assist with reports, presentations, educational materials, and other research-related projects.
- Participate in study-team and unit meetings and communicate progress, questions, and observations to the appropriate team members.
- Complete required institutional, privacy, safety, and research training, including applicable CITI and PEERRS modules.
- Maintain participant confidentiality, data integrity, and compliance with study protocols, institutional policies, and applicable regulations.
- Meet regularly with an assigned supervisor or mentor to receive guidance, discuss learning goals, and review progress
- Perform other related duties as assigned.
All activities will be performed within the intern’s documented training and authorization and under the oversight of qualified research personnel. Duties may vary based on unit needs, available learning opportunities, and the intern’s demonstrated competencies.
Supervision Received:
This position receives direct supervision and reports directly to the MCTSU Unit Administrator.
Supervision Exercised:
None
High school diploma or GED is necessary.
Bachelor’s Degree in Health Science or an equivalent combination of related education and experience is desirable. An understanding of medical terminology, experience in a large complex health care setting, ability to effectively communicate with staff and faculty of all levels, and knowledge of university policies and procedures is desirable.
The work requires, or the supervisor approves a fully…
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