Sr. VP, Head of Regulatory

Enveda

24d•$450,000 - $480,000•Remote

About The Position

Letâs build the future of medicine - together. Join Enveda as a Sr. VP, Head of Regulatory in a remote capacity and help us transform natural compounds into life-changing medicines. Weâre a team driven by curiosity and innovation - are you ready to make a difference? Remote | Full-time | $450,000-$480,000 What Makes Us Enveda Life is smart, and we can learn from it. Weâre reinventing drug discovery by harnessing natureâs intelligence. Our platform identifies new medicines four times faster than the industry standard because patients canât wait. What sets Enveda apart isnât just what we do - itâs how we do it. Our culture is built on creativity, collaboration, and deep respect for each other. We believe âPeople Create All Valueâ, and our success is driven by the extraordinary team turning our mission into reality every day. Weâre proud of the momentum weâve built. Our Momentum - 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: Americaâs Best Startup Employers (2024 & 2025) --Newsweek: Americaâs Greatest Startup Workplaces (2025) --LinkedIn: Top Startups to Watch (2024) These milestones reflect the impact of our team and weâre just getting started, but theyâre only possible because of the diverse talent, perspectives, and relentless drive of our team, and people like you. Your Role in Our Mission At Enveda, every role drives impact. As a Sr. VP, Head of Regulatory, youâll 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.

Requirements

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

Responsibilities

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