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Senior Director, Clinical Translational Science; Immuno-oncology

Job in Boston, Lincolnshire, PE21, England, UK
Listing for: GenepoolNetworks
Full Time position
Listed on 2026-10-10
Job specializations:
  • Research/Development
    Clinical Research, Oncology Care
Salary/Wage Range or Industry Benchmark: 140000 - 200000 GBP Yearly GBP 140000.00 200000.00 YEAR
Job Description & How to Apply Below

Summary Profile: Senior translational medicine leader with expertise in biomarker strategy, clinical pharmacology, and oncology drug development, capable of translating complex scientific data into actionable clinical and portfolio decisions.

Key Responsibilities
  • Lead translational medicine strategy across clinical development programs.
  • Develop biomarker and clinical pharmacology plans supporting target engagement, dose optimization, patient selection, and proof-of-mechanism.
  • Integrate biological, PK/PD, biomarker, and clinical data to guide development decisions.
  • Define translational milestones and biomarker strategies across the development lifecycle.
  • Partner with bioanalytical and laboratory teams on biomarker assay development and implementation.
  • Drive interpretation of translational data to understand mechanism of action, efficacy, and resistance.
  • Contribute to study design, protocol development, endpoints, and data analysis plans.
  • Collaborate with cross-functional teams, CROs, academic partners, KOLs, and vendors.
  • Support regulatory submissions and health authority interactions related to translational strategy and biomarkers.
  • Help build organizational capabilities while fostering a collaborative, patient-focused culture.
Qualifications
  • PhD, PharmD, MD, or MD/PhD in Immunology, Pharmacology, Molecular Biology, Clinical Science, Translational Medicine, or a related field.
  • Deep expertise in translational medicine, clinical development, and biomarker strategy.
  • Expertise in oncology, immunology and related therapeutic areas.
  • Track record advancing oncology programs from early clinical development through proof-of-concept and late-stage studies.
  • Proven ability to integrate scientific and clinical data to inform drug development and patient selection.
  • Experience leading cross-functional teams across Research, Clinical Development, and Regulatory Affairs.
Position Requirements
10+ Years work experience
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