Vice President Regulatory Affairs Jobs in Boston
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Search Results - Vice President Regulatory Affairs Jobs in Boston
Verastem Oncology-Boston
Position Summary
The Senior Vice President of Regulatory Affairs and Quality is a member of Verastem Oncology's leadership team and provides enterprise-wide leadership for global regulatory strategy and product quality. Working closely...
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Prime Medicine-Boston
CTAs, BLAs, MAAs, and related submissions to ensure timely filings
• Lead regulatory risk assessments and mitigation plans across the pipeline
• Represent regulatory affairs in executive discussions, due diligence for in-licensing, collaborations...
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Celea Therapeutics, Inc.-Boston
Celea Therapeutics is seeking an experienced Vice President of Regulatory Affairs to lead global regulatory strategy and serve as the primary FDA liaison as we advance deupirfenidone (LYT-100) through Phase 3.
This role reports to the Chief Medical...
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Entrada Therapeutics-Boston
Entrada’s pipeline, from preclinical through the clinical and registration stages. Reporting to the Senior Vice President, Regulatory Affairs, the successful candidate will support the development of strong internal processes, be the key liaison...
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Page Mechanical Group, Inc.-Boston
JOB TITLE: Executive Director, Global Regulatory Affairs
REPORTS TO: Vice President, Regulatory Affairs / Sr. Vice President, Regulatory Affairs
LOCATION: Boston, MA
DATE PREPARED: March 27, 2026
JOB SUMMARY:
The Executive Director, Global...
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Frontier Medicines-Boston
pharmacology leader, setting strategy and building out the function and will partner closely with Clinical Development, Regulatory Affairs, Biometrics, and CMC, bringing hands-on scientific expertise to trial design, dose optimization, and regulatory strategy...
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Verastem Oncology-Boston
Verastem Oncology seeks an accomplished Senior Vice President of Regulatory Affairs and Quality to lead global regulatory strategy and product quality for the company's small molecule portfolio.
This executive will set enterprise-wide priorities...
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Danaher Corporation-Boston
solving, and scalable audit practices across the BioPharma ecosystem.The Essential Requirements of the Job IncludeBachelor's degree in life sciences, quality, engineering, pharmacy, regulatory affairs, or a related field required; advanced degree...
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Tango Therapeutics, Inc-Boston
and their contribution to the ability of cancer cells to evade immune cell killing.
Tango's labs and offices are located at 201 Brookline Avenue, in the vibrant Fenway area of Boston, Massachusetts.
Summary
The Senior Vice President (SVP), Global & US Medical Affairs...
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US Pharmacopeia-Boston
advisor to pharmaceutical developers and manufacturers
• Create User Forums, Quality Hours, Workshops and Webinars with Scientific Affairs, Regulatory Affairs to showcase USP value
• Partner with regional distributors for aligned, resource-shared, joint...
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Danaher Corporation-Boston
Manager partners closely with Business Development, Legal, Contracts, Project Management, Manufacturing, Quality, Regulatory Affairs, Supply Chain, Technical Operations, Finance, and Executive Leadership to convert contractual commitments into executable...
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Premier Research-Boston
in pharma/CRO/biotech/consulting
• At least 7 years in a regulatory affairs management role
• Experience preparing regulatory submissions in US and/or Europe
• Experience with supervisory and financial management in regulatory affairs
• Proven track record...
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Amazon-Boston
Development, Regulatory Affairs/Manufacturing, and Commercialization — with demonstrated ability to translate industry dynamics into partner and business strategies
• 5+ years in Partner Management, Business Development, Strategic Alliances, or Consulting...
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Servier Pharmaceuticals-Boston
Excellence, Medical and Patient Affairs, Regulatory Affairs, Manufacturing, Finance, Legal and Compliance, Corporate Affairs and Global Commercial teams to ensure seamless execution of commercial strategy across the product lifecycle.
Primary...
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MSD-Boston
of Clinical Scientists in the execution of clinical studies.
• Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects
• Assist the Executive Director...
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