Allucent

Sr Medical Director/Executive Medical Director

🇺🇸 Zdalnie, Stany Zjednoczone Zdalnie Opieka zdrowotna i nauka Opublikowano Maj 19, 2026
Lokalizacja Zdalnie, Stany Zjednoczone
Tryb pracy Zdalnie
Język English
Opublikowano 19 maja 2026
Ostatnio sprawdzono 31 maja 2026
Kontekst JobGrid

Podsumowanie roli od JobGrid

Sr Medical Director/Executive Medical Director at Allucent: Zdalnie, Stany Zjednoczone; Opieka zdrowotna i nauka. JobGrid adds normalized role facts, source context, and a path to the employer application page so candidates can compare the listing before applying.

  • Location and workplace: Zdalnie, Stany Zjednoczone
  • Role classification: Opieka zdrowotna i nauka
  • Source freshness: checked by JobGrid on 2026-05-31.
  • Application path: candidates continue to the employer application page with non-personal referral tags.

We are seeking a Sr Medical Director/Executive Medical Director to provide medical leadership across Phase I–IV clinical development programs, serving as a trusted advisor to clients while driving clinical strategy, patient safety, and operational excellence. This is an opportunity to influence high-impact global studies within a dynamic, growth-focused organization dedicated to advancing drug development.

This role is based in United States(remote), either Part-Time or Full-Time.

 

About the role

As Executive Medical Director, you will play a critical role in shaping clinical development strategy and providing medical leadership across complex global studies.

Your main responsibilities will include but not limited to:

  • Advise sponsors on product development strategy, protocol design, endpoint selection, and clinical trial feasibility for Phase I–IV programs
  • Provide medical oversight and safety leadership for assigned clinical trials, including medical monitoring and safety review activities
  • Support business development efforts through proposal review, budget input, and participation in sponsor and bid pursuit meetings
  • Lead and support critical safety activities including SAE/SUSAR review, DSMBs, dose escalation meetings, and protocol deviation oversight
  • Review and ensure scientific integrity and medical consistency across key trial documents including protocols, ICFs, CSRs, DSURs, and PSURs
  • Mentor cross-functional teams and provide therapeutic expertise to internal stakeholders, investigators, and clients throughout study execution