Director, Regulatory Affairs Jobs in Princeton, NJ

Transform your career by providing expert guidance in regulatory affairs for innovative drug development. Lead the regulatory strategy for a diverse portfolio of biologics and large molecules while co...

Champion innovative regulatory strategies in a dynamic, global team dedicated to pioneering drug development. Leverage your expertise to navigate complex issues and deliver high-potential therapies ef...

Develop and drive regulatory strategy for clinical-stage programs, ensuring compliance with FDA and international guidelines. Collaborate with cross-functional teams to navigate complex regulatory lan...

Pioneer regulatory excellence by leading global product registrations, ensuring compliance, and guiding teams through complex submissions in the medical device sector for enhanced patient outcomes...

Join a team that's driving regulatory strategy for a leading product across multiple global markets. Oversee submissions and compliance, ensuring alignment with regulations while collaborating on prod...

Deliver impactful CMC regulatory support for IND/CTA development and maintenance, ensuring compliance and completeness across submissions while leading cross-functional collaboration and strategically...

Empower the development of CMC regulatory strategies for small molecule drugs. Lead global submissions and provide expert recommendations for meeting regulatory requirements, ensuring high-quality com...

Transform the regulatory landscape by managing CMC and clinical applications globally. Collaborate with stakeholders and health authorities to ensure expeditious approvals for clinical trials, emphasi...

Transform resource management in Regulatory Affairs by leveraging data to drive strategic workforce planning and enhance operational efficiency across a collaborative environment, ensuring optimal hea...

Empower your CMC expertise to drive global regulatory strategy and submissions, ensuring compliance during drug development and commercialization, while collaborating across regions to enhance patient...

Shape the future of regulatory strategy by leading projects that ensure compliance and market access. Drive collaboration across teams while managing processes for development and post-approval phases...

Transform regulatory affairs in oncology by leading strategic submission initiatives and cross-functional collaborations, ensuring compliance and quality for impactful development programs. Drive regu...

Unlock potential by leading regulatory submissions and ensuring compliance with FDA guidelines. Collaborate across teams to drive projects efficiently while coordinating with vendors. Your expertise w...

Unlock potential by leading regulatory affairs for advertising and promotions. Drive compliance with US and Canadian regulations while guiding cross-functional teams to achieve strategic business obje...

Drive regulatory compliance and quality management for global market access while enhancing your expertise in medical device regulations and expanding your leadership role in this dynamic, cross-funct...

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...

Optimize promotional compliance and strategy by leading regulatory initiatives across brands. Collaborate cross-functionally to ensure effective communication while mitigating risks within a dynamic p...

Lead and transform regulatory strategies for advertising and promotional activities in the US. Collaborate with cross-functional teams to ensure compliance with FDA regulations while supporting innova...

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...

Advance your career in regulatory advertising by leading compliance initiatives for promotional materials. Provide strategic guidance across teams, ensuring effective communications that satisfy FDA r...

Oversee the global pharma CMC regulatory team to ensure compliant product development and submissions, leading efforts in training, collaboration across departments, and acting as a liaison with regul...

Shape the future of global pharma CMC regulatory strategies by leading a dynamic team, collaborating cross-functionally, and ensuring successful pre- and post-approval submissions while developing rob...

Optimize global regulatory strategies for drug programs in cardiovascular metabolic areas. Lead cross-functional teams to secure approvals and navigate regulatory challenges effectively while fosterin...

Unlock potential by leading global regulatory strategies in cardiovascular and metabolic programs. Collaborate with cross-functional teams to ensure timely drug approvals while managing complex projec...

Lead the charge in global regulatory strategy development for innovative cardiovascular programs, ensuring efficient approval processes and strategic oversight to accelerate drug advancements through...