Latest Drug Regulatory Affairs jobs in Stoneham, MA

23 Drug Regulatory Affairs Jobs in Stoneham, MA

Executive Director, Medical Writing MapLight Therapeutics, Inc. - Burlington, MA, United States , in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms. What You’ll Do: Reporting to the VP, Regulatory Affairs 11 days ago
Director, Non-Clinical Toxicology MapLight Therapeutics, Inc. - Burlington, MA, United States Collaborate with CMC, Program & Portfolio Management, Clinical, and Regulatory Affairs to develop program-specific strategies for appropriate data generation in support of development candidate nomination, IND 14 days ago
Vice President, Oncology Breast Therapeutic Area Medical Head , NMD at Pfizer Pfizer - Cambridge, Massachusetts potential of our existing and future commercially available medicines. + The role will partner closely with Pfizer Oncology stakeholder groups (including Research, Early and Late Development, Regulatory 8 days ago
Senior Manager Regulatory Affairs, Strategy Inozyme Pharma - Boston, MA, United States of excellence, collaboration, and continuous learning. Qualifications: 1. Advanced degree (Ph.D., Pharm.D., or equivalent) in life sciences or a related field. 2. Minimum of 6 years of regulatory affairs 8 days ago
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Sr. Director of Regulatory Affairs - Oncology Mantell Associates - Boston, MA, United States sciences or a related field Minimum of 6 years of regulatory affairs experience in the biopharmaceutical industry, with a focus on rare diseases/oncology and orphan drug development Proven track record 9 days ago
Director, Regulatory CMC Editas Medicine - Cambridge, Massachusetts and advanced degree preferred with a minimum of 10 years’ experience in drug development/regulatory affairs and a minimum 8 years in CMC regulatory affairs. Experience with both US FDA and EMA with drugs 9 days ago
Validation Engineer (CSV) GQR - Waltham, MA, United States in computer system validation. Experience with computer systems supporting R&D functions such as Clinical, Pharmacovigilance/Drug Safety, Medical Affairs, Supply Chain, Regulatory Affairs, and Quality Assurance 8 days ago
CSV/ Validation Engineer Beacon Hill Staffing Group - Waltham, MA, United States , Pharmacovigilance/Drug Safety, Medical Affairs, Supply Chain, Regulatory Affairs and Quality Assurance is a plus Experience with ValGenesis is a plus Practical experience with quality risk management and risk-based 8 days ago
Pharmaceutical Program Manager The Fountain Group LLC - Cambridge, Massachusetts , Clinical Research, Regulatory, CMC, Marketing or other drug development related function Description: As part of the GMSO Program Management team, you will report to the Strategy & Operations Lead 4 days ago
Head of Drug Substance/CMC Lead Cellarity - Somerville, MA, United States development, medical affairs, new product planning, regulatory affairs, and corporate communications. Represent drug substance holistically internally and externally as needed. Activities include due diligence 17 days ago

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