Address
Form of workProvide 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: 24001431
- Daily Work Times: TBD
- Hours Per Pay Period: 80
- On Call: No
- Weekends: No
