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48279, Detroit, MI
Clinical Research Coordinator II

Sonic Summary

The position involves providing support as a study coordinator, data manager, and regulatory specialist for the Clinical Trials Office (CTO).
Candidates must have a Bachelor's degree or an equivalent combination of education and experience, with medical or science experience preferred.
The role requires managing study requirements, maintaining logs, and ensuring compliance with internal and external regulations.
Clinical research certification is preferred, and the position entails managing patient and protocol data while responding to queries promptly.
The salary for this position is not explicitly stated, but relevant experience in clinical trials is essential.

Position Summary: Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the clinical trials arena.

Responsibilities:

Assure all study requirements are met and documented and meet both internal and external regulations in accordance with protocol guidelines.

Maintain logs, including tracker submissions and update the CTO Oncore database in a timely manner according to CTO SOPs.

Design systems for coordinating, compiling and submission of data; design workflow processes and participate in quality assurance measures; coordinate site visits.

Manage all patient and/or protocol data as assigned and respond to queries in a timely fashion.

Schedule and participate in monitoring visits and participate in multidisciplinary team program meetings as required.

Qualifications:

· Bachelor’s degree required or equivalent combination of education and experience.

· Medical and/or science experience/education preferred.

· Clinical research certification preferred.

Equal Opportunity Employer of Minorities/Females/Disabled/Veterans

Learn more about this Employer on their Career Site

Clinical Research Coordinator II