Clinical Development Director

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