Job Description

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.

• 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.

• Bachelor's degree required or equivalent combination of education and experience.
• Medical and/or science experience/education preferred.
• Clinical research certification preferred.

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