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Clinical Research Coordinator I

Job Description

Clinical Research Coordinator I

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

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