VP, Head of Regulatory

Let’s build the future of medicine - together.

Join Enveda as a VP, Head of Regulatory in a remote capacity and help us transform natural compounds into life-changing medicines. We’re a team driven by curiosity and innovation - are you ready to make a difference?

Remote | Full-Time | $350,000-$400,000

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.

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: America’s Best Startup Employers (2024 & 2025)

Newsweek: America’s Greatest Startup Workplaces (2025)

Fast Company: Most Innovative Companies in 2026

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.

Your Role in Our Mission

At Enveda, every role drives impact. As a 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.

What You’ll Do

• 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