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Clinical Research Coordinator Pediatric Endocrinology
San Francisco is the primary location, will work in Oakland occasionally.
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.
Please address the following questions in a cover letter:
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.
Please address the following questions in a cover letter:
- 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 3-5 days per week and at UCSF Oakland Campus approximately 1-2 days per week?
- If selected for this position, when would you be able to start?
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