UCSF
Location
San Francisco, California
The Clinical Research Coordinator executes, manages, and coordinates research protocols under the direction of the Principal Investigator. They are responsible for coordinating data collection and operations for multiple concurrent clinical research studies while ensuring compliance with institutional and regulatory policies.
Candidates must have a high school diploma and sufficient experience to perform the assigned duties, along with strong communication and organizational skills. Proficiency in Spanish is required, and experience with clinical research systems or electronic medical records is preferred.
The Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
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