Senior Regulatory Affairs Specialist Jobs in Alameda, CA

Engage in supplier development initiatives that enhance quality, scalability, and process robustness. Lead cross-functional programs to improve supplier performance, reduce risk, and ensure long-term...

Accelerate supplier development by leading initiatives that enhance quality, scalability, and risk mitigation. Collaborate across teams to influence strategic procurement and ensure supply continuity...

Transform global CMC regulatory strategies for small molecules and biologics, leading submissions and interactions with health authorities. Oversee a team while ensuring compliance in all development...

Join a team that's dedicated to maintaining Good Clinical Practice and human subject protection. Oversee site monitoring, ensure compliance, and support clinical studies through effective communicatio...

Collaborate with clients and teams to manage projects, expectations, and delivery, ensuring high standards and strategic growth in a fast-paced medical affairs environment. Leverage experience to iden...

Lead regulatory support for Neurology and Oncology agents, driving strategies and submissions for global approvals. Collaborate across teams to enhance development timelines and ensure compliance with...

Help us drive product success in biopharma by managing lifecycle initiatives, collaborating cross-functionally, and supporting growth strategies to enhance profitability and customer satisfaction acro...

Take ownership of global regulatory and quality strategies for oncology programs. Lead a team to ensure compliance with FDA and global health authorities, supporting rapid execution of early-phase tri...

Elevate your career by leading compliance and quality in clinical trials. Collaborate with teams to ensure protocol adherence, site training, and resolve issues while maintaining high standards of mon...

Tackle clinical monitoring challenges while leading site initiatives for quality compliance and protocol adherence. Collaborate with cross-functional teams to ensure successful clinical trial executio...

Optimize your clinical research career by playing a vital role in overseeing and conducting site monitoring for clinical trials, ensuring compliance, quality, and effective team collaboration througho...

Unlock potential by leading site monitoring for clinical trials. Collaborate closely with cross-functional teams to ensure compliance, enhance recruitment, and oversee execution while providing guidan...

Champion innovative surgical technologies by leading regulatory strategies and shaping clinical evidence. Collaborate with cross-functional teams and senior leaders to navigate complex regulatory path...

Lead the charge in developing innovative regulatory approaches and managing multidisciplinary projects in California's Central Valley. Collaborate with clients and stakeholders to ensure successful pr...

Lead the charge in defining and executing the global compliance strategy for clinical development, fostering a quality-centric culture while ensuring adherence to regulatory standards and continuous i...

Lead the charge in establishing and optimizing global regulatory information management strategies. Drive operational excellence while collaborating with cross-functional teams to enhance submissions...

Join a team that's committed to enhancing product quality and safety through risk management, testing, and collaboration while driving compliance in a fast-paced, innovative environment focused on med...

Support quality initiatives by leveraging your expertise in Quality Systems. Collaborate with cross-functional teams to enhance product compliance and drive continuous improvement efforts within the m...

Shape a quality control framework for cancer registrars by conducting audits, providing essential feedback, and ensuring compliance with standards. Collaborate with a dedicated team to enhance data qu...

Transform the biopharmaceutical landscape by advising clients on regulatory compliance and clinical pharmacology strategies, leveraging your expertise to impact innovative drug development across dive...

Drive the global regulatory strategy for pioneering CAR-T therapies, engaging with health authorities to ensure timely filings and approvals while addressing risks and fostering collaboration across t...

Join a team that's shaping global regulatory strategies for microbial products, ensuring compliance across regions to support market entry and growth. This role involves strategic oversight, internati...

Join a team that's dedicated to enhancing clinical trial quality through leadership, mentorship, and oversight. Engage remotely with cross-functional teams, driving high standards for patient safety a...

Champion clinical trial quality by providing strategic leadership, oversight, and mentorship across multiple studies. Collaborate with cross-functional teams to ensure compliance, data integrity, and...

Elevate supplier quality through effective inspection processes and issue resolution. Collaborate with stakeholders to implement corrective actions and drive continuous improvement while ensuring comp...