Regulatory Affairs Specialist Jobs in Cambridge, MA

Elevate clinical outcomes by serving as the key pharmacist liaison among partners, translating real-world issues into actionable insights, driving resolution of clinical concerns, and enhancing produc...

Join a team that drives global regulatory strategy for innovative products. You will lead regulatory affairs for clinical development, ensuring alignment with health authority requirements and facilit...

Drive compliance excellence by overseeing regulatory adherence for complex benefit products. Collaborate with cross-functional teams, conduct risk assessments for innovations, and support escalations...

Drive impactful medical communication strategies by crafting precise scientific content and collaborating with cross-functional teams to meet diverse client needs within a dynamic healthcare landscape...

Drive compliance and legal support for regulatory affairs, guiding teams through complex healthcare laws while leading a high-performing legal group to enhance operational efficiency and navigate legi...

Unlock potential in medical device innovation through regulatory leadership. Drive compliance and approvals by collaborating with cross-functional teams to optimize strategies and influence successful...

Accelerate regulatory strategy development for oncology products, leading global initiatives to secure IND/CTA approvals and marketing applications. Collaborate with cross-functional teams to navigate...

Unlock quality assurance excellence by leading GxP documentation and training management. Enhance regulatory compliance and system efficiency in a cross-functional hybrid role within the pharmaceutica...

Join the operations and administrative team to enhance Medical and Clinical Affairs, managing programs and grants while ensuring efficient communication and project execution across various stakeholde...

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...

Join a team that's dedicated to ensuring product quality and regulatory compliance. The role involves batch record reviews, investigating deviations, and providing QA guidance to enhance GxP programs...

Drive quality assurance processes to support compliance and oversee QA operations. Collaborate on batch documentation, deviation investigations, and CAPAs, while enhancing GxP standards in pharmaceuti...

Join our dynamic Regulatory Affairs team to lead global strategies in drug development, ensuring impactful outcomes for innovative therapies in the Cardiovascular, Renal, and Metabolism sectors. Drive...

Lead the development of CMC regulatory strategies, ensuring successful product submissions and agency interactions. Collaborate with cross-functional teams to influence outcomes and maintain complianc...

Engage with key stakeholders to define CMC regulatory strategies, ensuring successful product delivery and first-pass approvals. Leverage expert insights to navigate complex submissions and foster str...

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...

Support compliance activities in manufacturing, ensuring adherence to regulations, quality standards, and effective communication across departments. Collaborate on training, CAPAs, deviations, and au...

Champion a comprehensive GVP quality program, partnering with multiple departments to ensure compliance through audits, training, and continuous improvement initiatives. Your expertise will enhance op...

Lead the charge in developing regulatory strategies for Specialty Surgery products, ensuring compliance across global markets, and driving cross-functional collaboration to achieve business objectives...

Lead the charge in shaping regulatory strategy for specialty surgery products, ensuring compliance with global requirements. Collaborate with cross-functional teams to drive innovative solutions while...

Advance your career with this executive leadership role overseeing regulatory strategy for a Specialty Surgery Division. Collaborate with cross-functional teams to ensure compliance and drive product...

Explore opportunities as a Clinical & Regulatory Information Management SME, supporting client delivery across VeevaRIM and Clinical initiatives. Engage with stakeholders, optimize processes, and enha...

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...

Drive quality assurance in GMP operations, ensuring compliance and product integrity while collaborating with internal and external stakeholders. Contribute to clinical manufacturing excellence throug...

Help us shape the future of clinical trials by providing regulatory guidance and maintaining compliance. Collaborate within cross-functional teams to ensure successful submissions and uphold industry...