Clinical Research Coordinator II- MT Pleasant, MI

Our take on this role

About this role

Coordinate study requirements, data management and regulatory documentation for the Clinical Trials Office at Karmanos Cancer Institute in Mt. Pleasant. Maintain study logs, update the Oncore database and coordinate site visits.

What could you bring from clinical work?

• Nurses: Your experience reviewing patient records and maintaining clinical documentation could help with managing study data and responding to queries.
• OTs and SLPs: Following standardized assessment procedures and documenting care may help you track study requirements and maintain documentation according to protocol guidelines.
• PTs: Experience collecting outcome data and maintaining standardized documentation could support designing study data workflows and participating in quality assurance measures.

Full job description from McLaren Health Care

Location: Mt Pleasant, Michigan

Karmanos Cancer Institute at McLaren Central Michigan
1221 South Drive
Mt. Pleasant, MI 48858

Job 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