# Director, Precision Diagnostics Oncology at GSK

GSK is hiring a Director, Precision Diagnostics Oncology. It pays $190k-$316k a year and Level rates it Little AI ●○○○; you can [apply on GSK](https://jobsbylevel.com/go/10e81271-8793-43d6-af17-850ee3a11993?utm_medium=ai-agent).

AI Level 1, AI centrality 37 out of 100. Remote (USA - Pennsylvania - Upper Providence).

## Details

- Company: [GSK](https://jobsbylevel.com/companies/gsk)
- AI level: AI Level 1 (score 37 out of 100)
- Location: Remote (USA - Pennsylvania - Upper Providence)
- Salary: $190k-$316k
- Posted: November 10, 2026
- Apply: https://jobsbylevel.com/go/10e81271-8793-43d6-af17-850ee3a11993?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=director-precision-diagnostics-oncology-at-gsk-4a6d10

## Description

Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together. Find out more: Our approach to R&D For candidates seeking to be located at our Stevenage site, this role will temporarily be based at Stevenage. However, the Company plans to relocate its offices to Cambridge, UK. The location of this role will therefore subsequently change to Cambridge, UK in accordance with timelines to be set by the Company. The relocation is currently proposed to take effect by early 2029. Director, Precision Diagnostics Oncology Position Summary In this Diagnostic Director role, you will implement diagnostic development encompassing technical, development, regulatory, commercial, and business development efforts according to agreed deliverables, timelines and budget. You will lead diagnostic projects and workstreams and partner cross-functionally with research, clinical development, regulatory, and commercial groups. You will help build and execute diagnostic strategies and solutions that align with oncology development needs. You will have the responsibility to deliver on the vision of equipping GSK to be a leader through innovation and diagnostic development driving value by treating the right patient with the right medicine. Responsibilities: - Execution of precision diagnostics strategy for oncology programs, spanning multiple assets and therapeutic areas. - Define diagnostic requirements for trials and, in partnership with clinical teams, implement biomarker selection, assay validation, and biological sample collection/handling strategy. - Oversee project plans, budgets, and timelines to ensure on-time, high-quality delivery of diagnostic milestones via cross-functional collaboration with project management, biomarkers, clinical & biomarker operations, external engagement, procurement, etc. - Work with regulatory and quality teams to ensure diagnostic development meets regulatory expectations and requirements and in diagnostic regulatory submissions. - Engage external partners, including diagnostic companies, clinical labs and technology vendors, to accelerate assay development and access to patient samples. - Provide frequent project status updates and reports related to diagnostic deliverables to the Diagnostic Subteam, in collaboration with project management, finance and business operations - Share learnings and best practices for diagnostic development and execution and participate in initiatives for key organizational process improvements. Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals: - Bachelor’s degree in life sciences, molecular diagnostics, clinical laboratory science, or related field. - 6+ years of experience in diagnostic development, direct experience in oncology is preferred - Demonstrated experience integrating diagnostics into clinical trial design and familiarity with clinical trial design elements such as efficacy endpoints, biomarker testing, data management and human biological specimen management and operations. - Knowledge of regulatory requirements for diagnostics or companion diagnostics (i.e. FDA, EU IVDR, PMDA/MHLW Japan, etc). - Protocol, informed consent and analysis plan development required to support diagnostic development and regulatory submissions - Proven ability to manage cross-functional projects, timelines, and budgets in a

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Source: https://jobsbylevel.com/jobs/director-precision-diagnostics-oncology-at-gsk-4a6d10

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