Clinical Research Coordinator - Neuroscape

University of California • San Francisco, CA

401d • $71,386 - $114,795

About The Position

The Clinical Research Coordinator at UCSF will independently manage and coordinate multiple clinical research studies, particularly focusing on psychedelic clinical trials. This role involves overseeing data collection, ensuring compliance with regulatory standards, and facilitating communication between various departments and stakeholders. The coordinator will also be responsible for managing study protocols, recruiting and training research staff, and maintaining data integrity throughout the research process.

Requirements

• High school graduation and sufficient experience and demonstrated skills to perform assigned duties.
• Strong attention to detail and excellent verbal and written communication skills.
• Ability to multi-task in a fast-paced environment and work independently.
• Experience with electronic medical records and knowledge of medical terminology.

Nice To Haves

• Fluency in the usage of Committee of Human Research (CHR) online iMEDris system.
• Understanding of patient population to create rapport and insight for patient participation.
• Knowledge of UCSF and departmental policies regarding research and confidentiality.
• Experience with database building/analysis and data management using platforms like Access, Stata, SASS/SPSS.

Responsibilities

• Execute, manage, and coordinate research protocols under the guidance of the Clinical Research Supervisor and/or Principal Investigator.
• Support the management and coordination of multiple psychedelic clinical research studies.
• Act as an intermediary between services and departments while overseeing data and specimen management.
• Manage and report on study results, creating and maintaining comprehensive datasets and reports.
• Coordinate staff work schedules, recruit and train volunteers and Assistant CRCs for the research team.
• Assist with oversight of other research staff and manage Investigator's protocols in the Committee on Human Research online system.
• Interface with sponsors and participate in the review and writing of protocols for institutional review board approval.
• Ensure compliance with all relevant regulatory agencies and maintain all regulatory documents.
• Report study progress to investigators and participate in internal and external audits or reviews of study protocols.

Benefits

• Comprehensive health insurance coverage
• Retirement savings plan options
• Paid holidays and vacation time
• Flexible scheduling options
• Professional development opportunities

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Educational Services
• Education Level: High school or GED