Director, Regulatory Affairs Jobs in Somerville, MA

Contribute to regulatory excellence by leading teams to develop successful strategies for biotech and pharmaceutical projects, ensuring compliance with FDA and global agencies while enhancing innovati...

Transform regional regulatory engagement by leading strategy, fostering relationships, and advocating for efficient electric transmission policies. Collaborate across departments to align regulatory g...

Champion regulatory excellence by leading global strategies for product approvals, collaborating with cross-functional teams and external experts to ensure compliance and drive successful commercializ...

Optimize regulatory CMC strategies for clinical and commercial products, leading cross-functional efforts to ensure compliance while monitoring global CMC trends and guiding teams through regulatory p...

Transform global regulatory strategies for oncology programs, leading cross-functional teams and ensuring timely submissions and approvals while developing high-caliber regulatory talent...

Lead the charge in advancing global CMC regulatory strategies for gene therapy products. Oversee lifecycle management, change management, and compliance to ensure successful post-approval activities w...

Drive impactful regulatory strategy and compliance to advance patient-focused missions. Lead and mentor within a dynamic team, ensuring alignment with organizational goals while fostering innovation a...

Lead regulatory strategies for CMC submissions and compliance in global projects. Collaborate with cross-functional teams to ensure accurate submissions and establish key relationships with authoritie...

Elevate regulatory compliance and market access by leading cross-functional teams to ensure safe, compliant strategies for diverse medical device products, driving innovation while navigating complex...

Accelerate progress at the forefront of global regulatory affairs by leading strategies for IND/CTA approvals, ensuring product launches, and executing post-marketing initiatives in the oncology secto...

Grow your career with a dynamic role guiding global regulatory strategies for biologics, collaborating cross-functionally while ensuring timely submissions and compliance within a fast-paced biotech e...

Lead the charge in developing innovative regulatory strategies for CAR-T therapies, collaborating with cross-functional teams and partners to ensure compliance and successful submissions worldwide, im...

Unlock potential by leading global regulatory CMC activities, developing strategies for product lifecycle management, and collaborating across teams to ensure successful agency submissions. Drive tran...

Drive impactful regulatory strategies in a fast-paced biopharmaceutical environment. Lead cross-functional collaboration for product development, ensuring compliance while advancing innovative solutio...

Lead the charge in global regulatory strategy for oncology programs, ensuring compliance and excellence in product registration. Partner with R&D and commercial teams to navigate complex regulatory la...

Drive compliance excellence in regulatory review and governance of promotional materials, ensuring alignment with FDA and FTC standards while leading cross-functional collaboration and operational imp...

Lead global regulatory strategy and ensure compliance across a complex portfolio, overseeing teams and driving submissions, approvals, and risk management in alignment with stakeholders and regulatory...

Unlock potential by leading regulatory CMC strategies for late-stage small molecule development. Collaborate with cross-functional teams to ensure compliance with global standards while driving qualit...

Champion innovative regulatory CMC strategies to guide global product development, ensuring compliance and facilitating interactions with health authorities while navigating complex projects in the ph...

Lead the charge in developing global regulatory strategies to secure market approval for products in assigned therapeutic areas, guiding cross-functional teams and ensuring compliance throughout the p...

Lead regulatory compliance for labeling and promotional activities in biotech, ensuring accuracy and adherence to regulations while collaborating across teams to shape strategic initiatives for produc...

Champion innovative regulatory strategies for rare disease programs, driving global initiatives from development through approval. Collaborate across functions to navigate complex landscapes and ensur...

Shape the future of regulatory excellence by managing global submissions, ensuring compliance across the drug development lifecycle, and collaborating across teams to facilitate strong health authorit...

Shape the future of regulatory strategy and execution, driving high-quality submissions and interactions with global health authorities throughout the drug development lifecycle, ensuring adherence to...

Champion global regulatory activities, ensuring high-quality submissions and strategic partnerships. Support lifecycle management across late-stage development, driving compliance with U.S. and intern...