Clinical Research Coordinator
About The Position
The Clinical Research Coordinator (CRC) will join a mission-driven research team dedicated to improving care for people with opioid use disorder (OUD) through innovative, patient-centered clinical research. This position provides an exciting opportunity to help launch and coordinate a pragmatic randomized controlled trial (RCT) comparing two approaches to buprenorphine initiation among people using fentanyl. The study is based at the San Francisco Outpatient Buprenorphine Induction Clinic (OBIC) and is a collaboration between UCSF, the San Francisco Department of Public Health, and community partners. The CRC will be part of a close-knit group committed to advancing health equity and expanding access to effective addiction treatment. Working under the direction of the Principal Investigator (PI) and research team, 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 study protocols. Responsibilities will include coordinating recruitment and enrollment, obtaining informed consent, managing study visits, collecting survey and clinical data, maintaining regulatory compliance, and ensuring smooth day-to-day study operations in accordance with UCSF and federal guidelines.
Requirements
- Perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate study protocols.
Responsibilities
- Coordinating recruitment and enrollment
- Obtaining informed consent
- Managing study visits
- Collecting survey and clinical data
- Maintaining regulatory compliance
- Ensuring smooth day-to-day study operations in accordance with UCSF and federal guidelines
Benefits
- Total compensation
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
