Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO).

 

 

Responsibilities:

 

Assure all study requirements are 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.  Respond to queries in a timely fashion.  Schedule and participate in monitoring visits and participate in multidisciplinary team program meetings as required.  Assist multidisciplinary team in research activities.

·         Bachelor’s degree required or equivalent combination of education and experience.

 

·         Medical and/or science experience/education preferred.

 

·         Proficient with the Microsoft suite including Excel and Power point.

 

·         Demonstrated attention to detail.

 

 

 

Equal Opportunity Employer of Minorities/Females/Disabled/Veterans

Additional Information Schedule: Full-time Requisition ID: 24006756 Daily Work Times: TBD Hours Per Pay Period: 80 On Call: No Weekends: No