Allucent

Sr Medical Director/Executive Medical Director

🇺🇸 Remote, Vereinigte Staaten Remote Gesundheit & Wissenschaft Veröffentlicht Mai 19, 2026
Standort Remote, Vereinigte Staaten
Arbeitsort Remote
Sprache English
Veröffentlicht 19. Mai 2026
Zuletzt geprüft 31. Mai 2026
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Sr Medical Director/Executive Medical Director at Allucent: Remote, Vereinigte Staaten; Gesundheit & Wissenschaft. 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: Remote, Vereinigte Staaten
  • Role classification: Gesundheit & Wissenschaft
  • 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