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

Additional Information Schedule: Full-time Requisition ID: 24001427 Daily Work Times: TBD Hours Per Pay Period: 80 On Call: No Weekends: No