Clinical Research Coordinator - Open Rank

Job description

Overview POSITION SUMMARY: Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator is responsible for independently performing delegated tasks and procedures involving human subject research. This work includes coordination of regulatory activities and aspects of collection and management of data for research protocols related to treatment, ancillary services, and prevention practices. This is an open-rank posting - candidates will be hired into the level commensurate with their experience. Responsibilities: ESSENTIAL FUNCTIONS: Clinical Research Coord I: - Obtain consent of research participants in accordance with the IRB approved protocols and all applicable regulations including HIPAA - Identify, schedule and/or conduct participant study visits, tests and/or interviews/telephone follow up calls - Coordinate participant remuneration/compensation per protocol - Maintain all regulatory documentation, including local or central IRB and study data. Provide data/support to study Investigators, sponsors and/or external monitors/auditors - Identify issues with protocol compliance. Keep principal investigator and manager aware of any issues r...