Research Study Coordinator III - Cancer Clinical & Translational Research - 40 Hours - Days
About the role
The Cancer Clinical and Translational Research Office (CCTRO) is the largest clinical research department at Henry Ford Health System. We manage approximately 200 ongoing trials that focus on the prevention, diagnosis, treatment and cure of cancer. Our staff have highly specialized roles in clinical coordination, research nursing, data management, regulatory coordination, grant management, and research sample processing. This is a fast growing program that is working with the Henry Ford Health and Michigan State University Health Sciences Partnership toward National Cancer Institute designation. The CCTRO is very team driven and passionate about providing high quality care to our patients and excellent support to our physician investigators.
Responsibilities
- Under minimal supervision, coordinate research projects within guides of regulatory compliance and/or Code of Federal Regulation.
- Provide technical support to Principal Investigators.
- Interact with internal and external customers at all levels.
- Oversee recruitment and coordinate day-to-day operations of the study.
- Have direct contact with potential and enrolled study participants.
- Provide other support as required.
- May work on multiple studies at any given time.
Requirements
- Education: Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology, or related field.
- Experience: Three (3) years of relevant experience with at least two (2) years of research project coordination experience.
- Certifications/Licensures: SOCRA or ACRP and IATA certification required.