Clinical Development Contractor

Let’s build the future of medicine - together.

Join Enveda in Clinical Development on a Contract basis 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 | Contract | $275-$350/hr |

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 Clinical Development contractor, you won’t just run a study you’ll own a clinical story.

What You’ll Do

Build the clinical thesis for for one of our programs from mechanism to endpoint, bringing deep disease expertise and regulatory fluency to every decision
Activate the site and KOL network the program can’t build without you, mapping the highest-value PI relationships needed for program success
Drive the thinking behind and execution of the overall study design and protocol
Lead clinical components of regulatory submissions and clinical activities
Lead the stakeholder dialogue to enable a high-quality Phase 2 study and drive clinical success,  including regulators, KOLs and Ad Boards, and patient advocacy organizations
Partner cross-functionally with clinical operations, translational, regulatory, and data science teams to move quickly from strategy to execution

We’re Looking For

MD, US-based - neurology or headache/migraine medicine expertise preferred; a recognizable name in the neurology clinical and research community
Live, warm global KOL and site network spanning headache medicine specialist centers
Track record of landing meaningful clinical readouts in neurology, pain, or metabolic conditions - ideally including at least one study where endpoint innovation was a core contribution
Fluency with the regulatory and endpoint complexity in chronic neurology indications
An undisputed champion for patients - someone whose decisions are always anchored in what is right for the people this program is designed to help
High-bandwidth, high-influence communicator who moves effortlessly across matrixed functions and builds alignment seamlessly
Strategic thinker with a pragmatic bias for action: clinical judgment grounded in rigorous science and a relentless quality-centric focus for patients
Entrepreneurial by nature: comfortable with ambiguity, energized by building, and motivated by impact over process
Lives Enveda’s values in practice - curious, direct, charitable with colleagues, and motivated by the journey over the destination