Senior Medical Director, Clinical Development, Hepatology

GlaxoSmithKline

Pennsylvania, US
Base: $284,625 to $474,375 (us); bonus/equity: ann...
Hepatology clinical development
Steatotic liver disease (sld) focus
Clinical trial design and execution
Provide clinical and scientific leadership for potential new, established and emerging indications for assets in clinical development with a strong focus on steatotic liver disease (SLD), including alcohol-associated liver disease (ALD)

Job Summary

  • Provide clinical and scientific leadership for potential new, established and emerging indications for assets in clinical development with a strong focus on steatotic liver disease (SLD), including alcohol-associated liver disease (ALD).
  • Contribute to the clinical development strategy for a drug or program and ensure execution of clinical development plans (CDP) for product(s) and/or indication(s).
  • This career opportunity requires an on-site office presence (minimum of two days a week) at one of GSK’s US (PA or MA) or UK (Stevenage or London HQ) sites.

Matching Summary

Provide clinical and scientific leadership for potential new, established and emerging indications for assets in clinical development with a strong focus on steatotic liver disease (SLD), including alcohol-associated liver disease (ALD).

Salary

Base: $284,625 to $474,375 (US); Bonus/Equity: annual bonus and eligibility for long-term incentive program; Benefits: health care, insurance, retirement, paid time off

Skills & Requirements

Must-have

  • Hepatology clinical development
  • Steatotic Liver Disease (SLD) focus
  • Clinical trial design and execution
  • Medical monitoring oversight
  • Global regulatory interactions

Nice-to-have

  • Innovative methodologies and processes
  • Enterprise mindset
  • Strategic thinking and problem-solving
  • Navigating ambiguity

Key Requirements

  • Medical degree and clinical medical specialty training board qualification/registration
  • Experience in global pharmaceutical/biotechnology industry
  • Experience in Hepatology drug development
  • Experience in late-stage clinical trials (Phase 2 and Phase 3)
  • Experience leading regulatory submissions
  • Matrix team experience

Work Rights

Not specified

Tailored Resume

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