Skip to main content
Enveda logo

Clinical Development Director

Enveda

Remote · USFull-time$225–250K/yrPosted todayStill listed today

Most applications go out cold — see where you stand first. No sign-up to start.

You apply on the employer's site, with no Olive account needed.

Watch jobs like this.

Don't just apply. Show up ready.

Olive works from this exact posting.

At a glance

Compensation
$225–250K/yr
Location
Remote · US
Schedule
Full-time
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Requirements

Credentials this posting asks for.

Doctorate, required

Job overview

The Clinical Development Director will lead clinical studies for Enveda’s oral medicines, owning work from protocol development through study start-up and enrollment. The role focuses on immuno-inflammation, including inflammatory bowel disease, and may span additional indications as the pipeline evolves. The director will collaborate with program heads, clinical operations, and medical monitors, using clinical, safety, and operational data to guide study decisions.

Skills & qualifications

RequiredNice to have

Skills

Clinical Development, nice to haveProtocol Writing, nice to haveClinical Study Leadership, nice to haveInflammatory Bowel Disease, nice to haveEndoscopic Endpoints, nice to haveCentral Reading, nice to haveData-Driven Judgment, nice to haveAI, nice to haveCollaboration, nice to havePatient-First Approach, nice to have

Qualifications

Advanced Degree or Equivalent, required8+ Years Clinical Scientist Experience or 3+ Years Industry After Clinical Training, requiredSecond Therapeutic Area Experience, nice to have

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match
Paid Time Off

Full job description

Let’s build the future of medicine - together.

Remote | Full time | $225,000 – $250,000

YOUR ROLE

As a Clinical Development Director at Enveda, you'll write the protocols and lead the studies for our first-in-class oral medicines, hands-on and across indications. Your role is within immuno-inflammation and will include inflammatory bowel disease, which is why experience there is preferred, and the role is built to work across indications as the pipeline needs. You'll report to the SVP of Clinical Development, and work day to day with the Global Program Heads, Clinical Operations, and the medical monitors. This is a high impact opportunity where you'll have the option to influence a growing program of clinical studies, across indications, whilst collaborating with some of the brightest minds in the industry and an AI-forward style.

WHAT YOU'LL DO

  • Own your studies end to end as their clinical lead, from protocol through start-up and enrollment

  • Write protocols and the clinical sections of regulatory documents yourself, making the study-level design calls and bringing endpoint, population, and go/no-go options to the Global Program Head with a recommendation

  • Work with Clinical Operations to hold CROs, sites, and vendors to timelines, enrollment, budget, and data quality, as the clinical voice in those conversations

  • Review blinded safety, PK, and operational data with the medical monitor and act on what it shows

  • Be flexible across decisions and across indications, collaborating and learning at speed as you move into new areas

  • Take on a study in a second indication when the pipeline needs it and get up to speed fast

  • Use AI every day in your own work to support you and build new ways of working, then share what works with the team

  • Build relationships with investigators, sites, and KOLs that make studies run well and designs stronger

  • Bring the patient's perspective into every consequential decision

WHAT WE'RE LOOKING FOR

  • An advanced degree (MD, DO, PhD, PharmD, or equivalent). Physicians and clinical scientists are equally welcome

  • Hands-on clinical development experience: you have written protocols as primary author and taken at least one study from protocol to database lock as its lead (typically 8+ years for a clinical scientist, or 3+ years in industry after clinical training for a physician)

  • Clinical or trial experience in inflammatory bowel disease, ideally with endoscopic endpoints and central reading (preferred, not required)

  • Experience in a second therapeutic area

  • Data-driven judgment: you turn clinical, safety, and operational data into clear decisions and change course when the data says to

  • AI-native or AI-ready: you are keen to learn, or already know how to, draft, check, and interrogate your own work with AI, and are aware of where it can mislead you

  • Ego-lite, high agency, and patient-first: collaborative, direct, no task too big or small, and never losing sight of who the trial is for

We hire for trajectory, not just credentials. If you meet most of the above and care deeply about this problem, we want to hear from you.

ABOUT ENVEDA

We're a clinical-stage, AI-enabled biotech discovering medicines from nature four times faster than the industry standard. We recently raised $311M in a Series E, bringing total funding to over $845M, and doubled our valuation to $2B. We now have three oral medicines in the clinic, including our lead drug, ENV-294, in Phase 2 trials for eczema and asthma. Forbes named us one of America's Best Startup Employers, and Newsweek recognized us as a Top 100 Most Loved Workplace. We're still early, and most of the best work is ahead of us.

Benefits (Starting Day 1): Medical, dental, and vision covered at 90%, 401(k) with company match, flexible PTO and a company-wide weeklong recharge break, adoption assistance

Our Process: We move fast and respect your time. Typically: a recruiter screen → hiring manager conversation → work sample, technical interview, & culture interview.

Our Values: Curiosity | Agency | Journey | Charity | Unity


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 [email protected].

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.

How this job compares

Set against the 510 open Clinical Development jobs on Olive Jobs, counted November 11, 2026.

Pay
  • This posting$225–250K/yr
  • US median$214–313K/yr440 salary ranges

This range's midpoint, $238K, is 9% below the US median midpoint ($261K) — in the middle half of Clinical Development salary ranges across the US.

Openings
Olive Jobs lists 510 open Clinical Development jobs across the US. 11% of them nationwide are listed as remote or flexible.
Hiring the most across the US
Experience
This posting asks for at least 3 years of experience — less than three in four Clinical Development postings that state a minimum ask for (median 6 years, across 435 postings).
Education
This posting asks for a doctorate or professional degree; 220 of the 510 open Clinical Development jobs (43%) ask for a doctorate or professional degree.

Counted across the open, public US postings on Olive Jobs on November 11, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

Prepare for this role

You've read the whole posting — now see how you match it.