On-Site Clinical Research Supervisor – Psychiatry Trials

University of California - Davis; California; On-site; USD 91,000 - 170,000; Full time

Job summary

University of California - Davis is seeking a Clinical Research Supervisor for the IMPACT Lab and Mood Disorders Research Program in the Department of Psychiatry and Behavioral Sciences. This on-site role leads multiple psychiatric trials, overseeing startup, recruitment, protocol execution, data quality, and regulatory compliance.

Under the PI, you will mentor staff, monitor performance, handle sponsor/IRB coordination, and drive workflows to ensure safety and timely study completion, budgets,

Qualifications

• CCRP/CCRC certification or equivalent required.
• Master's degree in a related field or relevant experience.
• Experience supervising clinical research staff.
• Budget development and extramural funding knowledge.
• Experience with GCP, IRB, and regulatory requirements.

Responsibilities

• Oversee day-to-day clinical research operations across concurrent studies, including startup, recruitment, and protocol implementation.
• Ensure data quality, regulatory compliance, sponsor and IRB coordination, monitoring, and study close-out.
• Train and mentor clinical research staff, assign and prioritize work, and develop standardized workflows.
• Support research budgets, grant and contract activities, reporting, and dissemination as assigned.

Skills

Supervision & mentorship

Leadership

Regulatory compliance

Data management

IRB/GCP knowledge

Communication skills

Education

CCR P/CCRC or equivalent certification

Master's degree in psychology/ neuroscience/ health sciences/ nursing/ public health or related field

Tools

EDC systems

MS Office (Word/Excel/PowerPoint)

Statistical analysis software

Job description

University of California - Davis is seeking a Clinical Research Supervisor for the IMPACT Lab and Mood Disorders Research Program in the Department of Psychiatry and Behavioral Sciences. This on-site role leads multiple psychiatric trials, overseeing startup, recruitment, protocol execution, data quality, and regulatory compliance.

Under the PI, you will mentor staff, monitor performance, handle sponsor/IRB coordination, and drive workflows to ensure safety and timely study completion, budgets,