Regulatory Affairs Specialist Jobs in Greenwich, CT

Build your expertise in our intensive 2-year rotational PharmD/PhD program, gaining critical skills through hands-on projects in Global Development while collaborating across diverse functional areas...

Execute the end-to-end delivery of clearinghouse product features, collaborating with cross-functional teams to enhance client experiences and ensure regulatory compliance while maintaining a focus on...

Collaborate with clients and teams to manage projects, expectations, and delivery, ensuring high standards and strategic growth in a fast-paced medical affairs environment. Leverage experience to iden...

Discover a pivotal role in establishing enterprise data stewardship standards, leading cross-domain collaboration, and ensuring consistency in planning data definitions and accountability across funct...

Join our team as a quality leader to enhance our Quality Management System, ensuring compliance with cGMP standards and readiness for audits. Drive continuous improvement and champion product quality...

Shape regulatory strategies that drive product innovation and compliance, ensuring alignment with FDA and global standards. Collaborate across teams to enhance product development and market entry in...

Join a team that's dedicated to maintaining Good Clinical Practice and human subject protection. Oversee site monitoring, ensure compliance, and support clinical studies through effective communicatio...

Elevate quality assurance and regulatory systems by managing daily operations, ensuring compliance, and supporting audits while collaborating on projects to enhance product quality and patient safety...

Champion a comprehensive GVP quality program, partnering with multiple departments to ensure compliance through audits, training, and continuous improvement initiatives. Your expertise will enhance op...

Take ownership of driving revenue growth and market share through strategic account management and consultative selling in the histology consumables sector, cultivating relationships with laboratory a...

Elevate our Histology Consumables business by driving revenue growth, expanding market share, and fostering strategic relationships with key stakeholders. Utilize your expertise to influence key busin...

Engage with laboratory leaders to drive strategic initiatives and revenue growth in the Histology Consumables sector. Build relationships, optimize account strategies, and leverage analytics to enhanc...

Unlock potential by executing financial and operational audits, identifying control deficiencies, and collaborating with stakeholders to enhance internal control environments through effective audit s...

Explore opportunities as a Clinical & Regulatory Information Management SME, supporting client delivery across VeevaRIM and Clinical initiatives. Engage with stakeholders, optimize processes, and enha...

Champion clinical trial quality by providing strategic leadership, oversight, and mentorship across multiple studies. Collaborate with cross-functional teams to ensure compliance, data integrity, and...

Drive quality assurance in GMP operations, ensuring compliance and product integrity while collaborating with internal and external stakeholders. Contribute to clinical manufacturing excellence throug...

Help us shape the future of clinical trials by providing regulatory guidance and maintaining compliance. Collaborate within cross-functional teams to ensure successful submissions and uphold industry...

Unlock potential in regulatory affairs by steering clinical trial submissions, ensuring compliance and strategic oversight. Collaborate with project teams, advising on regulatory pathways for successf...

Unlock potential by providing legal guidance for BaaS and payments initiatives, collaborating across teams to translate banking regulations into practical solutions, and ensuring compliance while fost...

Champion product innovation by providing legal guidance on BaaS and payments. Collaborate with cross-functional teams to navigate regulatory landscapes, ensuring compliance while fostering rapid growt...

Shape the future of medical devices by leading regulatory CMC strategies, ensuring compliance and collaboration across teams to drive the development of innovative combination products for patients wo...

Join a talented team focused on delivering high-quality international events. Lead project deliverables in meeting services, ensuring client satisfaction and adherence to budgets and timelines while f...

Serve as a key quality and compliance partner, overseeing audits, inspections, and CAPA management, while collaborating with cross-functional teams to ensure adherence to regulations and quality expec...

Drive technical evaluations of reimbursement projects, ensuring compliance and feasibility while collaborating with cross-functional teams to advance strategic recycling and operational priorities...

Empower innovation in quality compliance by overseeing GCP activities, conducting audits, managing regulatory inspections, and ensuring effective risk mitigation strategies throughout clinical develop...