enveda - Clinical Development Director
Requirements
• MD, with credentials that add actual and perceived credibility to the program • Live, warm global KOL and site network in autoimmune disease (metabolic disease as well is a plus) • Track record of taking assets into the clinic and landing non-trivial first-in-human and early-phase programs. Bonus points for at least one 'not just another X study' where design creativity was the unlock • First-hand experience designing and running early clinical development, particularly proof-of-mechanism studies in immune-mediated disease • Comfortable owning translational and pharmacodynamic strategy, not just trial logistics • Clinically creative and unlocked by clinical depth; strong strategic and scientific judgement • An undisputed champion for patients, someone willing to go to bat and change the paradigm, not just add another entry to it • The person colleagues call when they want a straight answer; well-regarded in the community in a substantive, not just social, way • Entrepreneurial by nature: comfortable with ambiguity, energized by building, motivated by impact over process • Ego-lite, Enveda culture: collaborative, direct, gets the work done without needing the spotlight • 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.
Responsibilities
• As a Clinical Development Director at Enveda, you won’t be working on another me-too drug. You’ll be working on a first-in-class opportunity with broad potential across metabolism and autoimmune disease, and it's one of the most exciting bets in our pipeline. You will own the core clinical development plan, design the first-in-human program, and build the path that turns a novel mechanism into a potentially transformational medicine in two therapeutic areas. This is a critical leadership role on the Asset team, where you will have a significant impact on its direction and success while collaborating with some of the brightest minds in the industry. • Let’s build the future of medicine - together. • Remote| Full-time | $330K–$370K • Build the clinical development plan and first-in-human strategy from the ground up • Design the Phase 1 protocol: dose, endpoints, population, pharmacodynamic readouts, and the design nuance of testing across two therapeutic areas, plus the operational realism to make it run • Shape the translational and biomarker strategy that turns a preclinical mechanism into a credible human proof-of-mechanism readout • Support the path to IND and the early regulatory strategy behind it • Run Advisory Boards that produce decision-grade insight and genuinely change how we approach trial design and next steps • Build the KOL and site network ahead of the clinic, so we're ready to move when the study opens
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