Director, Regulatory Affairs Jobs in Menlo Park, CA

Transform the future of patient safety by leading strategic safety monitoring and risk management initiatives for investigational and marketed products, ensuring compliance and collaboration across te...

Elevate clinical pharmacology strategy for cardiovascular development, leading cross-functional collaboration and ensuring regulatory submission excellence. This role demands strategic vision and exec...

Join our team to lead global safety strategies in pharmacovigilance, ensuring compliance and effective risk management across product lifecycles in Oncology and Neuroscience. Engage cross-functionally...

Deliver strategic leadership in GCP quality assurance, ensuring compliance across clinical development programs. Collaborate with cross-functional teams to maintain high standards and readiness for in...

Transform and oversee CMC leadership across global programs, ensuring timely execution of development, manufacturing, and commercialization strategies while driving alignment across cross-functional t...

Engineer regulatory strategies to navigate complex legislation, ensuring compliance in product submissions globally. Influence teams and lead cross-functional projects, while communicating effectively...

Champion Global Patient Safety operations by overseeing safety reporting, collaborating with internal and external teams, and ensuring compliance with regulatory standards across clinical programs. Dr...

Lead compliance for Medicare Advantage and ACO programs, overseeing regulatory adherence and operational excellence. Collaborate with internal teams and external partners to ensure effective complianc...

Join a dynamic team to manage regulatory CMC submissions, ensuring timely delivery and cross-functional alignment. Lead project planning, tracking, and stakeholder communication to drive successful ou...

Drive regulatory compliance and product approval processes for innovative medical devices. Collaborate across teams to develop strategies and submissions, ensuring adherence to global regulations whil...

Shape the future of U.S. trade and distribution; lead strategy, operationalize models, and build partnerships to ensure smooth commercial launches and product availability across diverse channels in a...

Empower clinical research strategies in neurology, leading complex studies and multi-disciplinary teams to deliver innovative therapies, while ensuring compliance with regulatory standards and excelle...

Champion clinical excellence by leading end-to-end execution of complex medical device studies, ensuring compliance, quality, and timely delivery while effectively managing resources, budgets, and cro...

Lead the development and execution of global clinical outsourcing strategies, ensuring alignment with corporate objectives while managing vendor relationships and optimizing operational efficiency thr...

Lead the charge in developing strategic medical content while collaborating cross-functionally and ensuring high standards of accuracy and clarity, influencing multiple therapeutic projects for a dive...

Shape the future of reimbursement project assessments by leading technical reviews, guiding analysts, and establishing impactful frameworks, standards, and processes. Collaborate cross-functionally to...

Lead the charge in regulatory approval processes, ensuring compliance globally while collaborating cross-functionally to present product registration documentation effectively and efficiently...

Optimize data collection and access across EDC/non-EDC sources. Drive compliance, manage vendor relationships, and ensure quality deliverables while contributing to clinical trial data processes and r...

Tackle procurement challenges by leading vendor negotiations, managing relationships, and ensuring compliance within a biotech framework. Drive efficiency in the procure-to-pay process while collabora...

Lead the charge in regulatory strategy and compliance, driving product approval and market access for innovative medical devices. Collaborate with cross-functional teams to ensure successful submissio...

Execute oversight of clinical product supply, ensuring compliance with global regulatory standards while managing cross-functional teams to mitigate risks and deliver quality materials to support AbbV...

Join a team that's committed to excellence in quality assurance. You'll lead GXP initiatives, ensuring compliance with global regulations while optimizing systems and processes to support pharmaceutic...

Drive the legal strategy for an innovative life sciences business, partnering with diverse teams to embed compliance and regulatory frameworks while promoting product development and market success...

Transform clinical operations by leading compliance management, ensuring adherence to regulations and protocols. Collaborate with cross-functional teams to streamline processes while promoting robust...

Partner with us to lead the strategic direction of our Medical Affairs, driving evidence generation, stakeholder engagement, and cross-functional collaboration to support oncology assets from late-sta...