About this Event
The CTO Clinical Research Investigator Foundations Intensive (a.k.a. PI Intensive) provides foundational information and resources for PIs conducting clinical trials at UCSF.
Instructor-led sessions are conducted on Zoom. Attending all modules is recommended, but not required.
Spring 2026
Day 1: Tuesday, April 14, 2026 | 9:00 AM - 2:00 PM
Day 2: Wednesday, April 15, 2026 | 9:00 AM - 2:00 PM
Things to note for Days 1 and 2:
Day 3: Thursday, April 16, 2026 | 10:00 AM - 12:10 PM
Things to note for Day 3:
Details for all 3 Days:
Before PI Intensive
CTO 300e: Foundations of Clinical Research (Online | On-demand)
This course reviews the foundations of clinical research at UCSF for PIs, including top PI responsibilities, best practices for protocol writing, training, manual of operations and procedures (MOPs), standard operating procedures (SOPs), documentation, checklists, and more. Resources for each topic are provided. Complete it here: CTO 300e: Foundations of Clinical Research.
Day 1
CTO 304: Hiring & Managing Research Staff
This course covers the role of research study team staff, best practices for estimating the amount and type of support needed for a research study, guidelines for sharing research staff effort with other PIs, navigating recruitment and onboarding, and managing study team staff.
CTO 303a: Pre-Award Tasks
This course covers basics of, and tips and tricks for, Pre and Post-Award tasks. Topics include: feasibility, pre-submission, study start-up, working with institutional partners including the Office of Clinical Trial Activation, coverage analysis, budgeting, and other details important to PIs conducting interventional research studies.
CTO 303b: Post-Award Tasks
This course provides a brief overview of study and financial award set-up, purchase orders, amendments, clinical research billing compliance responsibilities, study closeout, and more.
Day 2
CTO 301: Recruitment & Informed Consent + Workshop
This course covers the essentials of study recruitment, informed consent form (ICF) preparation, and best practices for performing an informed consent discussion. Additional topics include re-consent, documentation of the consent process, and more. Important details:
CTO 302: Adverse Events, Protocol Violations, & Incidents: Documentation & Reporting
This course covers best practices for identifying, documenting, and reporting (when necessary) the following occurrences: Adverse Events, Protocol Violations & Research Incidents, and other Safety-Related Information. It includes a review of the UCSF IRB’s requirements for reporting events and addresses how IRB reliances may impact reporting requirements.
Day 3
Best Practices in Community Engagement for Health Equity 101
This course is an interactive, introductory conversation focused on the foundational principles of meaningful community-engaged research. It explores the importance of positionality; clarifying the “who” and “why” of community engagement; and discusses best practices for identifying, approaching, and sustaining partnerships with vested community partners. CTSI’s Community Engagement Toolkit and consultation services are introduced, highlighting practical strategies attendees can use to strengthen inclusive research practices and deepen authentic collaboration with community.
If you have any questions about the CTO Training program, please contact us at CTO@ucsf.edu or reach out directly to Katie Aliféris, CTO Training Lead, at katie.aliferis@ucsf.edu.