Regulatory Affairs Specialist Jobs in New York, NY

Lead marketing initiatives for U.S. Injectables, collaborating cross-functionally to create promotional materials and drive campaign execution while ensuring compliance with regulatory standards and a...

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...

Lead the charge in ensuring compliance with banking regulations while managing risk assessments, audits, and policy governance. Collaborate cross-functionally to integrate controls and drive operation...

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...

Drive enterprise data stewardship by establishing standards, documenting business rules, and facilitating cross-functional alignment. Collaborate to ensure clarity and accountability in data definitio...

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...

Optimize medical writing deliverables for research projects ensuring clarity and compliance with regulatory standards. Collaborate across departments to deliver high-quality documents efficiently whil...

Unlock potential by providing strategic CMC regulatory expertise to accelerate the development and lifecycle management of drug-device combination products, ensuring compliance with global regulations...

Lead the charge in ensuring compliance for sterile and OSD manufacturing processes by managing batch reviews, documentation, and investigations, while training staff and participating in regulatory in...

Join a team that drives procurement excellence across global R&D operations. Support strategic sourcing and supplier management initiatives to enhance business value while collaborating with cross-fun...

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 global access programs for innovative cancer therapies, ensuring alignment with clinical, regulatory, and patient needs. Lead cross-functional teams to enhance early access strategy and opera...

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...

Help us drive product success in biopharma by managing lifecycle initiatives, collaborating cross-functionally, and supporting growth strategies to enhance profitability and customer satisfaction acro...

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...

Accelerate your career by leading negotiations for strategic contracts, aligning commercial goals with legal standards. Partner across teams to support growth, mitigate risks, and enhance customer sat...

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

Empower clinical trial excellence by leading oversight and mentorship of regional studies. Collaborate with cross-functional teams to enhance study execution while ensuring quality, compliance, and da...

Engage in leading clinical oversight and mentorship across regional trials, driving quality study execution while collaborating with cross-functional teams. This role emphasizes remote supervision, co...

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...