Clinical Research Coordinator I
McLaren Health Care
Date: 3 weeks ago
City: Detroit, MI
Contract type: Full time
Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO).
Responsibilities:
Additional Information
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.
Additional Information
- Schedule: Full-time
- Requisition ID: 25000971
- Daily Work Times: TBD
- Hours Per Pay Period: 80
- On Call: No
- Weekends: No
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