Clinical Research Support Specialist

2 weeks ago


Pittsburgh, United States University of Pittsburgh Full time
Key Responsibilities, but not limited to: Review clinical trial submissions from study team into central office for completeness. Work with study teams and/or sponsors to gather required documents to facilitate central office review process. Translate the protocol schedule of events (procedure/visit schedules) into CRMS system. Maintain spreadsheets and systems designed to track study information. Review IRB closure report and initiative close out process with research finance team. Monitor IRB submissions to ensure all studies have entered OCT workflow per policy. Monitor clinical research invoicing mailbox and route inquiries as appropriate.

  • Pittsburgh, United States University of Pittsburgh Full time

    Key Responsibilities, but not limited to: Review clinical trial submissions from study team into central office for completeness. Work with study teams and/or sponsors to gather required documents to facilitate central office review process. Translate the protocol schedule of events (procedure/visit schedules) into CRMS system. Maintain spreadsheets and...


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