Director, Global Real-world Evidence & Health Outcomes Scientist, Oncology

GSK

United States
Base: $204,000 to $340,000; bonus/equity: annual b...
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Health outcomes data
Real world evidence
Value evidence data
** GSK is seeking a Director of Global Real-world Evidence & Health Outcomes Scientist for Oncology, focusing on generating and maintaining health outcomes data to support product lifecycle management. The ideal candidate will have extensive experience in real-world evidence studies, particularly in oncology, and will collaborate across various teams to ensure robust evidence for market success. **

Job Summary

  • The role is critical to support the alignment of evidence with evidentiary requirements of customers responsible for marketing authorization, recommendation and reimbursement leading to successful patient access, product use and commercial success.
  • This role will provide YOU the opportunity to lead key activities to progress YOUR career.
  • Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

Matching Summary

Match Score: 75

** GSK is seeking a Director of Global Real-world Evidence & Health Outcomes Scientist for Oncology, focusing on generating and maintaining health outcomes data to support product lifecycle management. The ideal candidate will have extensive experience in real-world evidence studies, particularly in oncology, and will collaborate across various teams to ensure robust evidence for market success. **

Salary

Base: $204,000 to $340,000; Bonus/Equity: annual bonus and eligibility for share-based long term incentive; Benefits: health care, insurance, retirement, paid holidays, vacation, paid caregiver/parental and medical leave

Skills & Requirements

Must-have

  • health outcomes data
  • real world evidence
  • value evidence data
  • payer evidence
  • oncology or hematology experience
  • pharmaceutical industry experience

Nice-to-have

  • curiosity and continuous learning
  • clear communication
  • collaborative working style
  • rigour in methods
  • practical focus on timely evidence

Key Requirements

  • MSc or equivalent
  • 3+ years pharmaceutical industry experience
  • Experience planning and delivering projects
  • Experience designing RWE studies
  • Proficiency in utilizing evidence for HTA submissions
  • Experience communicating complex concepts

Work Rights

Not specified

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