Oncology Research Coordinator
CurrentCoordinates clinical, regulatory, business, and other research- related activities and documentation for clinical trials conducted, follows industry standards and applicable regulations including FDA/OHRP guidance, GCP and ICH.Essential FunctionsAssists with clinical, regulatory, business, and other documentation associated with oncology research projects/clinical trials within department.Participates in the study project start-up activity, works with the PI and others to initiate new research projects.Maintains protocol amendments, deviations, and informed consent changes regarding oncology research studies, assures all documentation is managed compliantly and maintained in an audit-ready manner.Maintains appropriate documentation for assigned studies.Assists in maintenance of filing systems, data repositories and systems.Assists in the monitoring of clinical trial compliance by reporting issues and problems appropriately.Obtains required documentation and to assess patient eligibility for research studies.Contacts local research staff to confirm scheduling of tests/treatments required by protocol.Obtains and completes data for patients enrolled on clinical trials.
