Senior Medical Director, Clinical Development, Advanced Pipeline Unit (apu), Hepatology

GSK

PA, US
If based in us (py or ma): $284,625 to $474,375; b...
Clinical development strategy
Clinical trial oversight
Hepatology drug development
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).
  • Stay abreast of advancements in therapeutic area research, clinical trial methodologies, competitive environment, and regulatory space to maintain GSK’s competitive edge.

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

If based in US (PA or MA): $284,625 to $474,375; Bonus/Equity: Annual bonus and long-term incentive program; Benefits: Health care, retirement, paid time off

Skills & Requirements

Must-have

  • Clinical development strategy
  • Clinical trial oversight
  • Hepatology drug development
  • Regulatory submissions
  • ICH and GCP guidelines

Nice-to-have

  • Innovative methodologies and processes
  • Enterprise mindset
  • Problem-solving skills
  • Strategic thinking

Key Requirements

  • Medical degree and clinical medical specialty training board qualification/registration
  • Experience in global pharmaceutical/biotechnology industry
  • Experience in clinical research and drug development
  • Experience in late-stage Hepatology drug development
  • Experience in medical monitoring activities
  • Experience leading regulatory submissions
  • Matrix team experience

Work Rights

Not specified

Tailored Resume

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