Diagnostic Delivery Lead

GSK • Upper Providence, PA

4d • $123,000 - $205,000 • Hybrid

About The Position

The Diagnostic Delivery Lead works within GSK’s Diagnostic Delivery Team in Oncology Translational Medicine, a group that delivers clinical diagnostic strategy across early- and late-stage oncology trials. The role owns operational delivery of diagnostics for assigned studies, from biosample collection and clinical trial assays at reference and central laboratories through to data that is ready for analysis, while maintaining audit readiness.

The role works in a matrix with Diagnostic Strategy, Biomarker, Clinical Operations, Data Management, Regulatory, Quality and Procurement colleagues, as well as external CROs, laboratories and vendors. The position is based in the United Kingdom with a hybrid working model. Applicants based at Stevenage will initially work there; GSK currently proposes to relocate its offices to Cambridge by early 2029, after which the role’s location will change to Cambridge according to the company’s timeline.

Requirements

• Bachelor’s degree in life sciences, biomedical science, or a related discipline.
• Experience in project or delivery management within diagnostics, clinical development, or healthcare settings.
• Knowledge of diagnostic technologies and their application in clinical trials or healthcare delivery.
• Understanding of regulatory requirements and quality standards relevant to diagnostics.
• Strong organisational and communication skills, with the ability to engage diverse teams and partners.
• Ability to manage multiple priorities and work in a fast-paced, matrix environment.

Nice To Haves

• Master’s degree or higher in a relevant scientific or healthcare discipline.
• Experience in pharmaceutical or biotechnology companies, especially in diagnostic or clinical operations roles.
• Familiarity with advanced diagnostic technologies or biomarker development.
• Experience managing vendor relationships and contracts.
• Demonstrated ability to contribute to process improvements and implement best practices.
• A collaborative and proactive approach to problem-solving and stakeholder engagement.

Responsibilities

• Implement diagnostic plans for oncology programmes in early- and late-stage development, maintain audit readiness, and identify, document and manage project risks.
• Define and deliver biosample collection, processing and storage for assigned studies, including input to laboratory manuals, kits and database setup; ensure logistical feasibility and cost-effectiveness; and forecast and manage biosample analysis and sample management costs.
• Manage implementation of clinical trial assays at reference laboratories, central laboratories and CROs, including contract execution and vendor oversight, and serve as the key contact for assay laboratories.
• Provide diagnostic input to protocols, informed consent forms and other study documents.
• Work with Clinical Operations on site communications and training materials, and train CRO and internal teams on sample collection and processing.
• Align with Data Management and Biostatistics on data requirements, contribute to data transfer agreements, and ensure data is ready for analysis.
• Serve as the first point of contact for biosample operational questions, resolve or escalate issues, and provide regular status updates, including sample tracking reports.
• Drive process and system improvements, coach and mentor colleagues as a subject matter expert, and role-model GSK values.

Benefits

• Annual bonus.
• Eligibility to participate in a share-based long-term incentive program, dependent on role level.
• Health care and other insurance benefits for employees and their families.
• Retirement benefits.
• Paid holidays.
• Vacation.
• Paid caregiver, parental and medical leave.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level