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Jobs(38,923)/Regulatory Affairs Manager Role(72)/enveda (10) - Sr. VP, Head of Regulatory
enveda

enveda - Sr. VP, Head of Regulatory

Remote - United States$450k - $480k4mo ago
RemoteVpNABankingPharmaceuticalsRegulatory Affairs ManagerSolutions ArchitectTeam ManagementDocumentationRegulatory Affairs

Responsibilities

• At Enveda, every role drives impact. As a Sr. VP, Head of Regulatory, you’ll be at the forefront of delivering hope to patients everywhere. Your expertise in global regulatory strategy will be critical in accelerating our mission to advance first-in-class small molecule and combination product programs because every breakthrough starts with bold questions and brave actions. • Let’s build the future of medicine - together. • Remote | Full-time | $450,000-$480,000 • What Makes Us Enveda • Life is smart, and we can learn from it. We’re reinventing drug discovery by harnessing nature’s intelligence. Our platform identifies new medicines four times faster than the industry standard because patients can’t wait. What sets Enveda apart isn’t just what we do - it’s how we do it. Our culture is built on creativity, collaboration, and deep respect for each other. We believe “People Create All Value”, and our success is driven by the extraordinary team turning our mission into reality every day. • We’re proud of the momentum we’ve built. • Unicorn status: Achieved following a $150 million Series D funding round in 2025 • Discovery and innovation: Advanced our first drug candidate to Phase 1 trials in 2024 • Award-winning culture: • -Newsweek: Top 100 Global #MostLovedWorkplaces (2025) • -Forbes: America’s Best Startup Employers (2024 & 2025) • -Newsweek: America’s Greatest Startup Workplaces (2025) • -LinkedIn: Top Startups to Watch (2024) • These milestones reflect the impact of our team and we’re just getting started, but they’re only possible because of the diverse talent, perspectives, and relentless drive of our team, and people like you. • Define and execute global regulatory strategies across early- and late-stage development for small molecules and combination products • Lead and oversee interactions with FDA, EMA, and other global regulatory agencies • Author, review, and submit key regulatory documents, including INDs, CTAs, briefing books, and response packages • Build and manage a high-performing regulatory team across strategy, operations, and publishing • ## We’re Looking For • Advanced degree (PhD, PharmD, MSc, or JD) in life sciences or regulatory sciences • 15+ years of global regulatory affairs experience in biotech/pharma, including successful submissions • Experience leading regulatory strategy for first-in-class or novel MOA products • Strong written and verbal communication skills with the ability to represent the company with regulators and external partners • If you’re passionate about innovation and impact, we encourage you to apply even if you don’t meet every requirement. • Our Values: Curiosity | Agency | Journey | Charity | Unity • Benefits: 90% Medical, Dental, Vision | 401k Match | Flexible PTO | Adoption Assistance • Enveda is protecting Job Seekers: • We care deeply about creating a safe, respectful experience for every applicant, so we wanted to share a few guidelines to help you spot anything that doesn’t feel right. • -You’ll always meet real Enveda team members through video or in-person conversations before receiving an offer. • -All communication from us will come from an @enveda.com or @envedabio.com email address. • -We’ll never ask you to purchase equipment, send money, or share sensitive banking details as part of any step in our recruiting process. • If something feels off or you’re unsure whether a message is truly from Enveda, please reach out at anytime at [email protected].

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