Clinical Research Coordinator II

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.

·         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