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

The Director, Global R&D Compliance will lead compliance guidance for R&D functions, ensuring adherence to regulatory standards, and developing effective policies and training. This role requires strategic advisory skills and collaboration with various stakeholders.

The Associate Director will lead the development of regulatory strategies, manage CMC submissions, and ensure compliance with health authority requirements for small molecules.

Support implementation of the Culture of Quality program, enhance Quality communications (webpage, newsletters, sessions), create a Quality department storyboard, produce graphic and digital content, collect and analyze data, and collaborate cross-functionally to advance quality initiatives.

The Associate Director will drive digital tool adoption, develop communication strategies, train users, monitor progress, and oversee AI capabilities in Quality processes.

Lead global strategic feasibility for clinical studies by integrating internal and external data, advising country/site selection, recruitment and operational strategies, improving feasibility processes and tools, and partnering with program and study teams to optimize study design and execution across early to late-stage programs.

Lead the U.S. Biologics Regulatory CMC organization, develop global CMC regulatory strategies, oversee CMC submissions and health authority interactions, manage a ~15-person team, ensure compliance and inspection readiness, and support lifecycle management for biologics including mAbs, ADCs, cell therapies, and combination products.

Support Privacy and Data Ethics counsel with legal research, policy and training drafting, contract and vendor reviews, privacy assessments, and project tracking to ensure compliance with global data protection laws (e.g., GDPR, HIPAA) across cross-functional teams.

The Executive Director leads Global Clinical Pharmacology & Development Technology Solutions, overseeing technology strategy, solution delivery, and team leadership to support R&D initiatives in cancer treatment.

The Sr Manager of Clinical Supply Chain oversees drug supply activities, manages relationships with stakeholders, ensures supply continuity, and leads process improvements.

The Manager of Clinical Supply Chain oversees drug supply activities, developing supply plans, managing inventory, and ensuring compliance with regulations while collaborating with internal and external stakeholders.