Clinical Research Coordinator I
Mclaren Healthcare
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: 24006614 Daily Work Times: TBD Hours Per Pay Period: 80 On Call: No Weekends: No
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