Offer summary

Qualifications:

B.S/B.A. degree preferred., 5+ years of experience in a pharmaceutical/biotech setting or CRO., At least 2 years of experience managing early phase clinical trials and CRO oversight., Excellent communication skills and strong knowledge of ICH/GCP/local regulations..

Key responsabilities:

Lead and manage one or more clinical trials, ensuring execution aligns with the clinical development strategy, budget, and timelines.

Author and review clinical trial documents, including trial-related plans and SOPs.

Oversee CRO activities and manage trial-related issues, ensuring compliance with regulatory requirements.

Job description

Let’s build the future of medicine—together.

Join Enveda as a Sr. Clinical Trial Manager 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 | $180,000 - $200,000

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: Forbes America’s Best Startup Employers

- Oct 2024: First drug to Phase 1 Clinical Trials

- Dec 2024: Raised a $130M Series C

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 Sr. Clinical Trial Manager, you’ll be at the forefront of delivering hope to patients everywhere. Your expertise in clinical trial management will be critical in accelerating our mission to bring innovative therapies to market—because every breakthrough starts with bold questions and brave actions.

What You’ll Do:

Lead and manage one or more clinical trials, ensuring execution aligns with the clinical development strategy, budget, and timelines.

Author and review clinical trial documents, including trial-related plans and SOPs.

Oversee CRO activities and manage trial-related issues, ensuring compliance with regulatory requirements.

Who will thrive in this role:

B.S/B.A. degree preferred with 5+ years of experience in a pharmaceutical/biotech setting or CRO.

At least 2 years of experience managing early phase clinical trials and CRO oversight.

Excellent communication skills and strong knowledge of ICH/GCP/local regulations.

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

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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