The Coordinator-Clinical Research 3 is responsible and accountable to oversee and coordinate the implementation and management of research trials. Coordinates investigator initiated as well as industry sponsored projects. Ensures protocol specific requirements are achieved through coordination of physician care, patient screening, recruitment, patient exams, investigational drug administration, accurate follow-up and documentation of patient's medical experience, and accurate documentation of research data. Serves as a lead and resource regarding research and compliance for investigators, nurses, and related clinical staff. Works independently under the supervision of the Principal Investigator (PI), and balances priorities upon receipt of project direction and focus from the PIs. Oversees and directs research projects, as designated by the PI. Performs other duties as needed.
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Job Type
Full-time
Career Level
Mid Level