Director, Regulatory Affairs Jobs in Watertown, MA

Help us drive strategic growth by cultivating partnerships with pharma and biotech firms. This role requires proactive relationship-building to enhance our clinical trials and expand our network acros...

Drive regulatory strategy for innovative mRNA products in oncology and rare diseases, navigating complex landscapes to ensure successful product development and approvals. Collaborate cross-functional...

Reimagine regulatory compliance by collaborating with engineering and product teams to integrate frameworks that ensure adherence to US and global standards across SaMD and AI/ML products. Your expert...

Partner with us to develop robust regulatory compliance frameworks for consumer, research, and SaMD products. Collaborate with cross-functional teams to embed compliance within the product lifecycle w...

Join a team that's driving innovation in drug development by leading cross-functional efforts for marketing authorization submissions. Collaborate effectively, manage project timelines, and ensure reg...

Drive compliance and product quality in medical devices by overseeing complaint handling and post-market processes. Collaborate globally to enhance regulatory adherence and lead improvements in qualit...

Transform strategic GPO agreements into operations, ensuring compliance and optimal product flow while managing performance metrics and safeguarding revenue integrity across the U.S. commercial channe...

Grow your career with a pivotal role in delivering engaging regulatory education to the insurance sector while building client relationships and collaborating with a dedicated team to ensure complianc...

Strategize your career as a Project Manager, overseeing clinical research studies, ensuring compliance with regulations, and driving team collaboration to meet trial milestones within set timelines. J...

Join a team that's dedicated to advancing clinical studies. As a Project Manager, you'll oversee the implementation of research protocols, ensuring compliance and effective communication across teams...

Engage with cross-functional teams to ensure regulatory compliance for Expanded Access Programs. Drive essential strategies and submissions while staying aligned with global legislation, impacting pat...

Lead the CMC regulatory strategy for biologics and ATMPs, overseeing resources and alignment with technical development. Foster collaboration for timely approvals and lifecycle progress in a fast-pace...

Oversee the regulatory strategy for biologics and ATMPs, driving global compliance and alignment across functions. Lead a team in managing submissions, approvals and lifecycle activities in a fast-pac...

Lead the charge in enhancing quality and compliance within Preclinical Safety by overseeing toxicology study data management and implementing innovative software solutions to streamline operations and...

Shape the future of regulatory strategies by leading US regulations for product development while ensuring compliance and fostering collaboration across global teams for successful market access and p...

Join a team that's redefining US regulatory strategies for product development, ensuring accelerated patient access through innovative pathways. Collaborate cross-functionally to represent and lead re...

Lead the charge in developing global regulatory strategies to ensure product compliance and alignment with corporate goals. Provide regulatory direction across programs, collaborate with stakeholders...

Join a dynamic team to drive CMC regulatory strategies and oversee submissions in the pharmaceutical sector. Lead experts in navigating complex regulatory environments while ensuring compliance and ef...

Join a team that's transforming compliance practices in the pharmaceutical sector. As a key partner, you'll guide business initiatives, ensuring they align with regulations while fostering collaborati...

Elevate global regulatory strategies as you lead cross-functional teams, ensuring compliance while driving market access for innovative products. Collaborate with stakeholders and health authorities t...

Drive global regulatory affairs for development teams, orchestrating activities and engaging both internal and external resources to ensure successful product registration and compliance with regulato...

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...

Provide comprehensive Regulatory Affairs support to ensure full compliance with U.S. FDA medical device regulations and international standards, facilitating product submissions and ongoing industry c...

Lead strategic regulatory consulting efforts for companion diagnostics, integrating insights across IVD development, clinical trials, and commercialization. Collaborate with stakeholders to ensure com...

Champion regulatory execution across gene editing programs, managing submissions, health authority interactions, and cross-functional collaboration to advance IND/CTA readiness and support impactful b...