Provide study coordinator / datamanagement / regulatory specialist support to the Clinical Trials Office (CTO).Manage independent assignment, providing excellent customer support andguidance 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.
- 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
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