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Clinical Research Coordinator III
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- POSITION SUMMARY:Under the general direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator III is responsible for independently performing delegated tasks and procedures involving human subject research.
- ESSENTIAL FUNCTIONS:Obtain consent of research participants in accordance with the IRB approved protocols and all applicable regulations including HIPAAAssist with recruiting, screening, selecting, maintaining and terminating study subjects for multiple protocolsIdentify, schedule and/or conduct participant study visits, tests and/or interviews/telephone follow up callsEnsure accuracy and completion of all regulatory documentation, including local or central IRB and study data.
- Assist with the training of staffDevelop preliminary designs for study related documentation of data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)Contribute to grant preparation, assessment of protocol feasibility, manuscript writing, data presentations and Institutional Review Board (IRB) processesAssist with financial /operational aspects of grant and contracts.
- Keep principal investigator and manager aware of any issues regarding complianceComply with all safety and infection control standards appropriate to this positionAdhere to Good Clinical Practice (GCP) guidelines and all human subject protection practicesPerform other duties as required.
- Help us set up our laboratories and get our studies running efficiently as we move our research programs from other institutions to Umass!
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