Regulatory Affairs Specialist Jobs in Durham, NC

Join a dynamic team to provide comprehensive regulatory support across clinical, submission, and post-approval phases for pharmaceutical products, ensuring compliance with global regulations while man...

Shape the future of drug development by leading nonclinical regulatory strategies and engagements. Collaborate with multidisciplinary teams and clients to drive clinical progress, ensuring compliance...

Elevate your expertise by joining a dynamic team that drives nonclinical regulatory strategies for drug, biologic, and vaccine development, ensuring advancement from discovery to clinical approval whi...

Lead the charge in developing strategic nonclinical regulatory pathways that accelerate medical product advancements, partner with multidisciplinary teams, and navigate complex regulatory landscapes t...

Reimagine global compliance strategies as you guide regulatory submissions, assess product impacts, and collaborate across teams to ensure adherence to medical device regulations while enhancing quali...

Join a team that shapes global regulatory strategy in a fast-paced environment. You will lead comprehensive regulatory plans, ensuring alignment and execution from development to post-marketing, impac...

Reimagine Regulatory Affairs by leading complex outsourcing programs and driving client success. Utilize deep expertise in strategy and operations to manage projects, mentor teams, and deliver tailore...

Drive regulatory excellence by managing submissions, guiding teams, and ensuring compliance. Utilize your expertise to support global projects and foster collaboration in a fast-paced environment focu...

Lead the charge in global regulatory strategies for innovative medical devices, driving project success from registration to compliance. Collaborate across teams to enhance healthcare technologies and...

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...

Join a team that manages site activation processes, ensuring compliance with regulations and SOPs. Collaborate with project teams to maintain timelines, oversee deliverables, and provide expert guidan...

Collaborate with cross-functional teams to drive regulatory strategies and manage submissions for drug products. Provide expert guidance to ensure compliance and oversee regulatory activities througho...

Engage with a dynamic team to facilitate regulatory operations for novel therapeutics. Drive submissions to FDA/CVM while collaborating across multidisciplinary teams to set new regulatory standards i...

Take ownership of QA and compliance systems, driving continuous improvement and regulatory adherence through audits, product reviews, and cross-functional collaboration within the site to ensure inspe...

Lead the charge in transforming global regulatory strategies into successful outcomes. Oversee regulatory activities and empower teams to ensure quality compliance, timely delivery, and robust cross-f...

Engage with regulatory authorities as you oversee the process of acquiring and maintaining essential pesticide registrations. Collaborate with cross-functional teams to ensure compliance and drive inn...

Drive global regulatory labeling initiatives, ensuring compliance and quality of documentation across diverse markets. Lead strategic governance, influence policies, and collaborate cross-functionally...

Join a team that's shaping regulatory strategies for pharmaceutical products. Lead CMC regulatory activities, collaborate with cross-functional teams, and provide guidance. Actively mentor junior staf...

Join a dynamic team driving regulatory CMC strategies to advance innovative treatments. Collaborate with cross-functional teams while mentoring junior staff and managing complex regulatory submissions...

Drive regulatory strategy by collaborating cross-functionally to influence promotional activities, ensuring compliance while optimizing risk management for impactful business decisions across a dedica...

Join our team to lead regulatory strategies across major programs, driving impactful submissions and fostering collaboration within a challenging and dynamic environment. Embrace the opportunity to in...

Join a team that's dedicated to advancing regulatory strategies for innovative SaMD products. Collaborate cross-functionally to drive compliance, manage documentation, and ensure readiness for audits...

Shape the future of quality assurance in manufacturing by ensuring compliance with regulatory standards, conducting audits, mentoring teams, and driving continuous improvement initiatives in a complex...

Unlock potential by leading regulatory CMC strategies for oncology products, coordinating submissions, and collaborating across teams to ensure compliance and successful product registration in a dyna...

Manage and lead comprehensive validation activities in a GMP environment, ensuring compliance with FDA and EMA standards. Collaborate with cross-functional teams while mentoring junior staff and maint...