VP, Head of Regulatory
This position is no longer accepting applications(closed Aug 16, 2026).
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
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
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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 recruiting@enveda.com.
At Enveda, we’re building a place where everyone can do the best work of their life. We are an equal opportunity employer and value diversity in all its forms. Apply now and join a team committed to shaping the future of drug discovery.
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- (Transcription) - Candidate experience will always be top priority for Enveda. We would like to offer you the opportunity to have your virtual interviews transcribed. This will allow your interviewer to spend less time notetaking and more time being present and engaged with you. In addition, transcriptions may help to expedite feedback so you will know what is happening with your candidacy sooner. You can opt out at any time which will not affect your candidacy. Opting in enables you to request a copy of the transcription. choose one · optional
- Describe your experience in developing and executing global regulatory strategies for small molecules and combination products. Please include examples of early and late development stages. written answer
- Provide an example of a regulatory challenge you anticipated in a previous role and explain how you developed a mitigation strategy in collaboration with clinical, CMC, and nonclinical functions. written answer
- Explain your approach to leading the authoring, review, and submission of key regulatory documents, including INDs, CTAs, briefing books, and response packages. Include details on ensuring alignment with program milestones and strategic objectives. written answer
- Describe your experience in building and managing a high-performing regulatory team, including internal staff and external partners. How do you ensure operational excellence within your team? written answer