Top Tech Jobs & Startup Jobs in San Francisco Bay Area, CA

The Director, Global Product Leader oversees product development programs, manages cross-functional teams, and ensures strategic alignment for regulatory and commercial processes in the pharmaceutical industry.

The Associate Director of Project Management will lead oncology program execution, drive cross-functional collaboration, manage timelines, and provide strategic support to ensure successful project outcomes.

The Director of Quality Systems will manage QA projects, implement regulatory risk management strategies, and ensure compliance with pharmaceutical quality standards while leading a team in a collaborative environment.

The Manager, Centralized Start-Up will lead informed consent review and study start-up activities, ensuring compliance and collaboration across teams.

Lead drafting, review, negotiation, and administration of commercial and G&A contracts. Partner with Commercial, Medical Affairs, Finance, and Compliance to improve CLM processes, templates, and workflows. Oversee contract execution, provide stakeholder guidance, manage intake and recordkeeping, and support CLM system design and training.

Lead commercial FP&A for forecasting, gross-to-net, expense planning, and performance analysis. Partner with Commercial, Accounting, NPP, and S&OP to drive forecast accuracy, ROI analysis, purchase order controls, and strategic financial recommendations for senior leadership.

Lead mechanistic modeling (PBPK/QSP) to support IND-enabling decisions and FIH dose selection; integrate preclinical, biomarker, and early clinical data; oversee population PK/PKPD and exposure-response analyses; contribute to regulatory submissions; mentor staff and build internal pharmacometrics capabilities while partnering cross-functionally.

The Senior Director, Global Privacy leads the privacy governance strategy, ensuring compliance with global privacy laws, overseeing privacy risk management, and guiding senior executives in data use governance.

The Associate Manager oversees centralized monitoring for clinical trials, focusing on risk management, data surveillance, and regulatory compliance while ensuring quality and participant safety.

The Associate Director, Quality Assurance oversees GCP QA operations, conducts audits, supports clinical study activities, and ensures compliance with GCP regulations.