Lead Medical Director, Product Development, Cvrm

Roche UK

San Francisco, CA, US
Base: $233,500 - $433,600; bonus/equity: discretio...
Board certified md in gastroenterology or hepatology
3+ years biopharmaceutical clinical development experience
3+ years medical monitoring experience in life sciences
The Lead Medical Director leads the development of Clinical Development strategies and ensures effective execution for assigned molecules in late-stage trials

Job Summary

  • The Lead Medical Director leads the development of Clinical Development strategies and ensures effective execution for assigned molecules in late-stage trials.
  • This role requires significant collaboration with internal partners including business development, research, commercial, and legal teams to drive label-enabling outcomes.
  • Relocation support is provided for this position based in San Francisco, Boston, Welwyn, or Basel.

Matching Summary

The Lead Medical Director leads the development of Clinical Development strategies and ensures effective execution for assigned molecules in late-stage trials.

Salary

Base: $233,500 - $433,600; Bonus/Equity: Discretionary annual bonus available; Benefits: Standard benefits package detailed at link provided

Skills & Requirements

Must-have

  • Board Certified MD in Gastroenterology or Hepatology
  • 3+ years biopharmaceutical clinical development experience
  • 3+ years medical monitoring experience in life sciences
  • 2+ years engaging with clinical sites and KOLs
  • Solid understanding of Phase II-III drug development

Nice-to-have

  • Outstanding interpersonal and influencing skills
  • Experience with outcome trial designs
  • Ability to foster inclusive team-based culture
  • Strong scientific writing and presentation skills

Key Requirements

  • MD (MBBS) Board Certified/Eligible in Gastroenterology/Hepatology
  • 5+ years post-grad clinical/scientific research experience
  • 3+ years experience in biopharmaceutical clinical development
  • 3+ years medical monitoring experience within life sciences
  • 2+ years experience engaging with PIs and KOLs

Work Rights

Not specified

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