Director, Clinical Pharmacology

Let’s build the future of medicine - together. 

Join Enveda as a Director, Clinical Pharmacology in a Remote position 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 | $200,000 - $250,000

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: 

- Jan 2024: Named a LinkedIn “Top Startup to Watch” 

- Mar 2024 & Mar 2025: Forbes America’s Best Startup Employers 

- Oct 2024: First drug to Phase 1 Clinical Trials 

- Aug 2025: Raised 150M Series D, gaining Unicorn status

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 Director, Clinical Pharmacology, you’ll be at the forefront of delivering hope to patients everywhere. Your expertise in clinical pharmacology strategy will be critical in accelerating our mission to safely and effectively translate compounds into clinical development because every breakthrough starts with bold questions and brave actions.

• Lead clinical pharmacology strategy across early- and late-stage clinical programs, including dose finding and exposure–response modeling. 
• Oversee PK/PD study design, analysis, and interpretation, collaborating with clinical operations, biostatistics, and regulatory colleagues. 
• Act as the subject-matter expert for clinical pharmacology in regulatory submissions and interactions with the FDA/EMA.

• PhD, PharmD with experience in DMPK, Clinical Pharmacology or a related discipline. 
• 15+ years of experience in biotech or pharma, with a strong track record leading clinical pharmacology efforts in drug development. 
• Demonstrated expertise in PK/PD, modeling & simulation, dose finding, and exposure-response strategies.

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