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Recruiting study participants (., identifying and screening potential subjects, obtaining informed consent); Coordinating patient visit schedules as per study protocol, including ensuring ongoing informed consent; Executing or coordinating all aspects of study visits (., assessment of adverse events, monitoring safety, medication admin...
About the Role
Job Description
The Research Coordinator will work closely with the principal investigators to oversee all research activities, primarily in the Divisions of Critical Care and Neurology, Department of Medicine, and act as the liaison between Physicians, the Accelerating Clinical Trials (ACT) Consortium, participants, and study sponsors as needed. The contract is initially for 12 months, with the potential for annual renewal and continuous employment.
Ongoing training for all active research protocols and amendments, in addition to the study delegation log for specified responsibilities:
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