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From the employer's careers site First seen 1 Nov 2026

Director, Oncology Translational Medicine, Clinical Biomarkers

GSK Stevenage Hybrid senior full-time

Salary

$189,750 to $316,250 per year

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Description

The Director, Oncology Translational Medicine, Clinical Biomarkers is responsible for developing and implementing biomarker and translational medicine strategies to support late-stage oncology assets.

As a key member of a Clinical Matrix Team (CMT), the Clinical Biomarker Director will collaborate with the Clinical Biomarker Executive Director to establish clear decision-making criteria, define patient segmentation strategies, and integrate these into clinical development plans.

Key responsibilities:

  • Collaborate with the Clinical Biomarker Executive Director to drive the design, alignment, and execution of clinical biomarker and translational medicine strategies.
  • Validate and implement biomarker strategies, including target engagement, pharmacodynamic, and proof-of-mechanism biomarkers.
  • Participate in tumor-specific Biomarker Matrix teams and execute clinical biomarker strategies for late-stage oncology programs.
  • Represent Translational Medicine at Clinical Development Matrix Teams (CMT) to establish biomarker-driven decision-making criteria.
  • Support disease area strategies and translational objectives by defining biomarker priorities and generating decision-enabling evidence packages.
  • Identify cutting-edge science and technological advances to incorporate into biomarker strategies.
  • Oversee and develop sample testing plans and deliver high-quality biomarker data packages.
  • Manage effective relationships with cross-functional teams.
  • Support the expansion of mechanism and disease understanding to generate insights for indication expansion.
  • Define and study mechanisms of resistance to enable reverse translation and inform next-line strategies.
  • Contribute to the company's scientific credibility through publications and presentations.

Basic Qualifications:

  • Ph.D. or equivalent with 7+ years or M.Sc. with 10+ years of drug development experience in the pharmaceutical industry.
  • Solid background in Oncology clinical biomarkers, expertise in late-phase oncology studies, and translational research within clinical development.
  • Strong expertise in cancer biology and clinical development.
  • Experience in leading cross-functional teams and designing and executing strategic biomarker plans.
  • Experience conducting clinical trials and working as part of clinical study teams.
  • Experience designing and executing translational biomarker plans for clinical trials.

Preferred Qualifications:

  • M.D., Ph.D. or equivalent doctoral degree in a relevant scientific discipline.
  • Experience with high-dimensional dataset analysis.
  • Prior experience with diagnostic development and regulatory interactions.
  • Experience with digital pathology, AI/ML-enabled biomarker analyses, external scientific partnerships, and mentoring or developing scientific colleagues.

The annual base salary for new hires in this position ranges $189,750 to $316,250. The position offers an annual bonus and eligibility to participate in a share-based long-term incentive program. Available benefits include healthcare and other insurance benefits, retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.

Skills

Required

  • Analytical Thinking
  • Clinical Data Interpretation
  • Clinical Data Review
  • Clinical Development
  • Clinical Trial Designs
  • Clinical Trials Monitoring
  • Digital Fluency
  • Drug Regulatory Affairs
  • Executive Presence
  • Hematology and Oncology
  • Learning Agility
  • Matrix Leadership
  • Real World Evidence (RWE)
  • Scientific Presentations

Nice to have

  • high-dimensional dataset analysis
  • diagnostic development
  • regulatory interactions
  • digital pathology
  • AI/ML-enabled biomarker analyses
  • external scientific partnerships
  • mentoring or developing scientific colleagues
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