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GSK

Director, Oncology Translational Medicine, Clinical Biomarkers

GSK

. Develop and implement biomarker and translational medicine strategies for late-stage oncology assets .

Posted 10/26/2026full-timeUpper Providence • Pennsylvania • United StatesLead💰 $189,750 - $316,250 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in developing and implementing biomarker strategies for late-stage oncology assets, with a strong background in oncology clinical biomarkers and translational research. Proficient in managing cross-functional teams and executing clinical biomarker plans while ensuring alignment with regulatory strategies.

Highest-signal resume keywords
Ph.D. Or EquivalentOncology Clinical BiomarkersLate-Phase Oncology StudiesTranslational ResearchFlow Cytometry

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Drug Development ExperienceClinical Trials ExecutionBiomarker Plan DesignHigh-Dimensional Dataset AnalysisGenomic AnalysisTranscriptomic AnalysisProteomic AnalysisRegulated Biomarker AssaysPatient StratificationMechanism Of Resistance
Soft Skills
Interpersonal SkillsCommunication SkillsProblem-Solving SkillsProject Management SkillsPresentation Skills
Tools & Technologies
NGSFISHPCRIHC/IFLiquid Biopsy/CtDNAAI/ML-Enabled Biomarker AnalysesDigital Pathology
Industry Keywords
Translational MedicineClinical DevelopmentBiomarker Matrix TeamsTherapeutic LandscapesSolid Tumor MalignanciesHaematological MalignanciesDecision-Enabling Evidence PackagesScientific ExchangeExternal Scientific PartnershipsClinical Study Designs

About the role

Key responsibilities & impact
  • Develop and implement biomarker and translational medicine strategies for late-stage oncology assets
  • Collaborate with the Clinical Biomarker Executive Director to establish decision-making criteria and patient segmentation strategies
  • Validate and implement target engagement, pharmacodynamic, and proof-of-mechanism biomarkers
  • Support patient stratification, dose selection, and clinical go/no-go decisions
  • Participate in tumor-specific Biomarker Matrix teams and execute clinical biomarker strategies
  • Represent Translational Medicine on Clinical Development Matrix Teams and integrate biomarker criteria into clinical study designs
  • Define biomarker priorities and generate decision-enabling evidence packages using real-world, internal, and external data
  • Identify scientific and technological advances for indication selection, patient enrichment, and combination strategies
  • Oversee or develop sample testing plans and deliver biomarker data packages for clinical development and regulatory strategies
  • Manage relationships with clinical and scientific operations, diagnostics, medical science, medical affairs, regulatory, portfolio management, and commercial functions
  • Support mechanism and disease understanding for indication expansion and scientific exchange
  • Define and study mechanisms of resistance to inform next-line strategies, patient enrichment, and asset life-cycle management
  • Contribute to scientific credibility through publications and presentations

Requirements

What you’ll need
  • Ph.D. or equivalent with 7+ years of drug development experience in the pharmaceutical industry, or M.Sc. with 10+ years of drug development experience
  • 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
  • Knowledge of therapeutic landscapes, approved and investigational agents, and diagnostic approaches in solid tumor and haematological malignancies
  • Experience leading cross-functional teams
  • Experience designing and executing strategic biomarker plans, including regulated biomarker assays
  • Experience conducting clinical trials and working as part of clinical study teams
  • Experience designing and executing translational biomarker plans for clinical trials
  • Experience collaborating with Data Sciences to analyze high-dimensional preclinical and clinical data
  • Hands-on experience with flow cytometry, NGS, FISH, PCR, IHC/IF, liquid biopsy/ctDNA, and multi-omic biomarker analyses
  • Experience translating preclinical research to human clinical trials using genomic, transcriptomic, and proteomic analyses
  • Track record of influencing teams and key leaders
  • M.D., Ph.D. or equivalent doctoral degree in a relevant scientific discipline would be advantageous
  • Experience with high-dimensional dataset analysis, diagnostic development, regulatory interactions, digital pathology, AI/ML-enabled biomarker analyses, external scientific partnerships, and mentoring scientific colleagues would be advantageous
  • Excellent prioritization, planning, timely execution, interpersonal, communication, problem-solving, project-management, and presentation skills

Benefits

Comp & perks
  • Annual bonus
  • Eligibility to participate in share-based long-term incentive program
  • Health care and other insurance benefits for employee and family
  • Retirement benefits
  • Paid holidays
  • Vacation
  • Paid caregiver/parental and medical leave
  • Comprehensive benefits program