Regulatory Director Jobs
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Regulatory Affairs Director Ad/Promo
Director of Regulatory Affairs, Ad/PromoSalary: $188,000-$235,000 Summary:A leading biotech in Burlington, MA is seeking a dynamic and visionary Director of Regulatory Affairs for Advertising and Promotion. In this influential role, you'll partner with diverse cross‑functional teams to shape compelling, compliant promotional strategies that elevate...
Senior Director Regulatory Affairs
EPM Scientific are partnered with a cutting‑edge biotechnology company is seeking a Senior Director of Regulatory Affairs to lead global regulatory strategy across a portfolio of innovative, high‑impact programs. This team is composed of world-class scientists and innovators who are leading the charge on integrating advanced imaging and AI technolo...
Senior/Principal Scientist, LBA
Senior Scientist / Principal Investigator, Bioanalysis & Biomarkers(GLP/GCLP · LBA · PK/ADA/Biomarkers)Overview A leading CRO is seeking an experienced bioanalytical scientist to join its Bioanalysis & Biomarkers group. This team supports global pharmaceutical and biotech partners by delivering high‑quality GLP/GCLP bioanalysis, method development,...
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Senior Director Regulatory Strategy
A cutting‑edge biotechnology company is seeking a Senior Director, Regulatory Affairs to lead global regulatory strategy across a portfolio of innovative, high‑impact programs. This team is composed of world-class scientists and innovators who are leading the charge on integrating advanced imaging and AI technologies to revolutionize drug discovery...
Associate Director Regulatory Affairs
Associate Director / Director Regulatory AffairsConfidential Early‑Stage Biotech | San Diego, CA (Onsite Preferred / Hybrid Considered)Expected Compensation: $180-$200k base + bonus + equityWe're supporting a confidential, venture‑backed RNA therapeutics company in San Diego. They're backed by top-tier global biotech investors, and developing a pip...
Regulatory Affairs Director
Regulatory Affairs Lead / DirectorWe are looking for an experienced Regulatory Affairs professional to guide US and EU regulatory strategy for a complex medical device.What you will do* Lead the full US market entry strategy including 510k, De Novo or PMA routes * Run Q Sub and Pre Submission processes and prepare all submission documents * Act as ...