Regulatory Compliance Coordinator
||72320 Oncology Research
||Full Time 40 HRS
Responsible for submitting protocols to the Institutional Review Boards for research and maintaining accurate protocol files. High School graduate or equivalent with general business courses. Prefer two to five years experience as administrative assistant.
Essential Functions and Job Duties: Coordinate and/or prepare material for timely submission to IRB for the research office.Organize and maintain protocol files,including central office,physician offices,radiation oncology,pharmacy and DMH oncology dept,disseminate protocol documents to appropriate staff in timely manner.Keep accurate records of protocol activities and IRB submission.Complete and maintain drug accountability log forms for DMH pharmacy and the CCSCI pharmacy. Collaborate with other staff to ensure all protocol information organized and completed. Back up to other Regulatory Compliance Coordinators in their absence.Prepare records for audit.
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