Regulatory Affairs Specialist Jobs in Greenwich, CT

Unlock potential by leading site monitoring for clinical trials. Collaborate closely with cross-functional teams to ensure compliance, enhance recruitment, and oversee execution while providing guidan...

Innovate robust global regulatory frameworks to enhance compliance, drive quality initiatives, and support strategic goals across diverse teams while ensuring adherence to international standards and...

Drive regulatory excellence in product innovation, ensuring compliance and safety while empowering creativity and strategy across teams in a dynamic, collaborative environment. Be the key connector be...

Join a pivotal role in regulatory affairs, guiding promotional materials in compliance with FDA and provincial guidelines in a dynamic, remote environment. Lead the Materials Review Committee and shap...

Join a dynamic team to execute financial and operational audits, ensuring robust controls and collaborating with clients to enhance audit effectiveness and integrity...

Lead quality assurance and compliance for Specialty Claims operations, ensuring adherence to regulatory standards and best practices. Collaborate with team members to enhance processes and deliver ins...

Oversee quality compliance and aseptic operations, managing staff and processes to ensure regulatory adherence, risk assessment, and continuous improvement in a GMP environment...

Shape your career by leading the regulatory strategy for critical global products. Collaborate with cross-functional teams to ensure compliance and successful submissions while managing asset developm...

Transform regulatory strategies and drive innovation in digital health devices by collaborating cross-functionally to ensure compliance, optimize processes, and support global product development init...

Innovate with cross-functional teams to shape regulatory strategies for digital health and medical devices, ensuring compliance and streamlined processes for product development and market entry acros...

Elevate medical affairs through expert coordination and strategic collaboration in investigator-initiated research, medical education, and post-market activities to enhance compliance and internal ope...

Shape the future of regulatory strategy by leading cross-functional teams, driving innovative development strategies, and providing regulatory thought leadership to ensure compliance and accelerate pr...

Join as a Clinical Research Associate to oversee critical monitoring tasks across diverse clinical studies. Ensure high-quality standards while facilitating communication between project teams and sit...

Drive data transformation into actionable insights supporting product quality and patient safety. Leverage statistical analysis, AI, and analytics to proactively identify trends, enhance decision-maki...

Unlock your potential by managing ISCC compliance for renewable fuels, overseeing regulatory risk, and ensuring audit readiness. Collaborate with cross-functional teams to drive sustainability and com...

Elevate quality management by leading compliance strategies for sterile injectables, ensuring regulatory adherence, and fostering a culture of continuous improvement across global operations while col...

Join us to lead global regulatory strategies in the Vaccines and Infectious Disease area, ensuring compliance and optimal approval timelines. Collaborate cross-functionally, directly engage with regul...

Lead the development of global CMC regulatory strategies and manage eCTD submissions for investigational and marketed products, collaborating with cross-functional teams to support lifecycle managemen...

Transform regulatory writing by leading complex submissions, mentoring teams, and ensuring compliance. Drive innovation and improve processes while collaborating across teams to enhance product succes...

Innovate the future of regulatory labeling by driving strategies across global teams, ensuring compliance and quality at all stages of product development while collaborating with key stakeholders to...

Drive global CMC regulatory strategies and submissions for clinical and commercial products. Collaborate cross-functionally to ensure compliance, lifecycle management, and timely delivery of high-qual...

Empower healthcare data integration by executing interface projects and collaborating with teams to ensure successful deployments. This role offers a great opportunity for detail-oriented individuals...

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

Shape the future of financial technology by driving quality assurance initiatives for sophisticated exchange and clearing platforms. Collaborate with cross-functional teams to implement robust automat...

Transform healthcare data integration by managing complex projects with minimal guidance. Collaborate with cross-functional teams to solve client issues, optimize data flows, and ensure successful go...