Director, Oncology Clinical Pharmacology, Modeling And Simulation

GSK

Cambridge, MA, US
Base: $188,100 to $313,500; bonus/equity: annual b...
Phd in quantitative clinical pharmacology
5+ years mechanistic pkpd modeling
Proficiency in nonmem or r
This role focuses on delivering quantitative excellence to inform the development of innovative Oncology therapies by ensuring they reach the right patients at the right dose

Job Summary

  • This role focuses on delivering quantitative excellence to inform the development of innovative Oncology therapies by ensuring they reach the right patients at the right dose.
  • The position requires defining and executing model-based development strategies for oncology projects while applying innovative methods such as drug-disease modeling and AI/ML informed analyses.
  • GSK offers a supportive environment for scientists to contribute to business decisions through innovation, expertise, and influence with a mission to impact the health of 2.5 billion people.

Matching Summary

This role focuses on delivering quantitative excellence to inform the development of innovative Oncology therapies by ensuring they reach the right patients at the right dose.

Salary

Base: $188,100 to $313,500; Bonus/Equity: Annual bonus and share based long term incentive program eligible; Benefits: Health care, retirement, paid holidays, vacation, and parental leave

Skills & Requirements

Must-have

  • PhD in Quantitative Clinical Pharmacology
  • 5+ years mechanistic PKPD modeling
  • Proficiency in NONMEM or R
  • 3+ years clinical data analysis experience
  • Expertise in AI/ML applications

Nice-to-have

  • Oncology research and development experience
  • Strong drive and learning agility
  • Experience with senior stakeholders
  • Track record of MIDD implementation
  • Excellent interpersonal communication skills

Key Requirements

  • PhD in Quantitative Clinical Pharmacology or Life Sciences
  • Master degree with 4+ years relevant experience
  • 5+ years utilizing mechanistic PKPD skills
  • 3+ years planning and reporting clinical data analysis
  • Verifiable proficiency in NONMEM or R tools

Work Rights

Not specified

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