UCSF
Location
San Francisco, California
The Clinical Research Coordinator independently manages and coordinates research protocols, ensuring regulatory compliance and data quality. Responsibilities include overseeing multiple clinical studies, supporting IRB submissions, and coordinating staff activities while adhering to institutional policies.
The position requires experience in clinical research and the ability to manage multiple studies and competing priorities. Candidates must be available for a 40-hour work week with occasional evening and weekend hours and be able to work on-site at specified UCSF campuses.
Work will be on-site in both UCSF Benioff Children’s Hospital in San Francisco (Mission Bay) and UCSF Benioff Children’s Hospital in Oakland.
The Clinical Research Coordinator (CRC) independently manages and coordinates research protocols under general direction. Responsibilities include overseeing multiple clinical studies, ensuring regulatory compliance, managing data and documentation, supporting IRB submissions, maintaining data quality, coordinating staff activities, and participating in audits while adhering to UCSF policies and research guidelines.
What skills and experience do you have that make you a good fit for this position? Describe your experience with research, clinical trials, working with patients, children, families, or diabetes. Describe your organizational skills and provide an example of how you handle competing priorities. What are your plans for the next 2-3+ years (are you planning to go back to school, if so, what program/timeline for matriculation, etc.)? Do you speak any other languages? If so, which one(s)? The hours are generally 40 hours per week, with some occasional evening and weekend hours. Are you able to commit to this schedule and be on-site at UCSF Mission Bay Campus approximately 2-3 days per week and on-site 2-3 days per week in Oakland, based on the needs of the studies? If selected for this position, when would you be able to start?
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