September 29, 2025
Neurology
Full Time
Req Number:
86280BR
Supervises staff involved in routine research study coordination. Receives predetermined work assignments that are subject to a moderate level of control and review. Oversees staff in execution of assignments; trains and mentors staff to improve quality and quantity of work.
This Clinical Research Supervisor is responsible for overseeing set up and management of Schedule I Phase 2 investigator-initiated behavioral pharmacology studies and sites as well as large multi-site, Phase 2 and 3 sponsor-driven pharmacology projects under several PIs within the Neuroscape Psychedelic Division, Psychiatry Department and at the SFVA. Involves the development of and ensures compliance with clinical study protocols that involve human subjects in complex clinical research studies with Schedule 1 compounds. Oversees and resolves operational aspects of clinical studies or trials in conjunction with project teams and in accordance with standard operating procedures and good clinical practice and regulations. May be responsible for finances, clinical operations,resource management and site and vendor selection. responsible for supervising, training, onboarding, coordinating, monitoring, managing, and overseeing the activities and schedules of a growing number of psychedelic facilitators and physicians, CRCs, Assistant CRCs, research assistants and volunteers. Serves as a hiring manager, responsible for determining staffing needs across these projects, interviewing candidates and responsible for managing resource distribution and personnel efforts across studies and across departments.
This Clinical Research Supervisor is responsible for overseeing set up and management of Schedule I Phase 2 investigator-initiated behavioral pharmacology studies and sites as well as large multi-site, Phase 2 and 3 sponsor-driven pharmacology projects under several PIs within the Neuroscape Psychedelic Division, Psychiatry Department and at the SFVA. Involves the development of and ensures compliance with clinical study protocols that involve human subjects in complex clinical research studies with Schedule 1 compounds. Oversees and resolves operational aspects of clinical studies or trials in conjunction with project teams and in accordance with standard operating procedures and good clinical practice and regulations. May be responsible for finances, clinical operations,resource management and site and vendor selection. responsible for supervising, training, onboarding, coordinating, monitoring, managing, and overseeing the activities and schedules of a growing number of psychedelic facilitators and physicians, CRCs, Assistant CRCs, research assistants and volunteers. Serves as a hiring manager, responsible for determining staffing needs across these projects, interviewing candidates and responsible for managing resource distribution and personnel efforts across studies and across departments.
The final salary and offer components are subject to additional approvals based on UC policy.
Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.
The salary range for this position is $164,300 - $399,100 (Annual Rate).
To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html
