Clinical Research Coordinator II
McLaren Health Care•Flint, MI
About The Position
Provide study coordinator, data management, and regulatory specialist support to the Clinical Trials Office (CTO). Manage an independent assignment while providing excellent customer support and guidance in the clinical trials arena.
Requirements
- Bachelor’s degree or an equivalent combination of education and experience.
Nice To Haves
- Medical and/or science experience or education.
- Clinical research certification.
Responsibilities
- Ensure study requirements are met and documented in accordance with protocol guidelines and internal and external regulations.
- Maintain logs, including tracker submissions, and update the CTO Oncore database promptly according to CTO SOPs.
- Design systems for coordinating, compiling, and submitting data; design workflow processes; participate in quality assurance measures; and coordinate site visits.
- Manage assigned patient and/or protocol data and respond to queries in a timely manner.
- Schedule and participate in monitoring visits and attend multidisciplinary team program meetings as required.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
