Associate Director, Clinical Operations

Role Summary

Associate Director, Clinical Operations responsible for independently leading global and complex clinical trials. Lead the Study Management Team, oversee clinical vendors and CROs, and ensure successful execution of clinical trials. Directly manage a large complex early-phase oncology study, including vendor selection, protocol development, feasibility/start-up, maintenance, and closeout. Located in San Francisco with an expectation of at least 3 days per week in office.

Responsibilities

• Provide strategic input and leadership in study set-up and execution of highly complex oncology clinical trials. May support multiple trials
• Establish and continuously monitor study timelines and budgets, promptly escalating significant risks or changes, as appropriate
• Develop and manage study contracts, budgets and timelines
• Author/review core study documents including protocol and Informed Consent Forms
• Manage CRO, c...