Biotechnology Jobs

• Stevenage
• £74,250 – £202,125 pa
• Lead

Joins the Genomic Technologies group within Translational Sciences, working in an existing Statistical Genetics team. Develops and tests production methods for analysing large-scale human genetic data, integrating genetic association data across omic and phenotypic layers to identify causal genes, drug targets and biomarkers. Collaborates with Data and Predictive Sciences, Biostatistics, AI/ML and disease area teams to influence portfolio decisions.

PySpark · BigQuery · Docker +3

• Cambridge
• US$205,425 – US$342,375 pa
• Lead · manages people

Senior technical authority leading GSK's Forward Deployed Engineering function, setting enterprise standards for AI-native development while owning delivery outcomes for a portfolio of strategic business units. Stays hands-on across architecture, ML and agentic engineering, leading Staff and Senior FDEs on precedent-setting engagements and acting as escalation point for the hardest technical decisions.

Claude Code · GitHub Copilot · Databricks AI Assistant +4

• Waltham, United States
• Hybrid
• US$123,000 – US$205,000 pa
• Lead

Owns operational delivery of diagnostics across early and late-stage oncology trials, from biosample collection and clinical trial assays at reference and central labs to audit-ready data. Works in a matrix with Diagnostic Strategy, Biomarker, Clinical Operations, Data Management, Regulatory, Quality and Procurement, plus external CROs, labs and vendors, and mentors colleagues as a subject matter expert.

CRO

• Ware
• Lead

Leads analytical strategy for late-phase small molecule products, owning comparability studies, characterisation strategies and specification/stability recommendations across the post-approval lifecycle. Partners in a matrix with R&D, GSC, Technical and Regulatory, defends analytical product strategy in health authority inspections and embeds method knowledge into tech transfers.

PAT

• King of Prussia, United States
• Lead

Leads analytical strategy for late-phase small molecule products, owning comparability studies, characterisation strategies and post-approval change submissions. Partners across R&D, manufacturing sites and regulatory in a matrix, embedding method knowledge into tech transfers and defending strategies during health authority inspections.

PAT

• Rockville, United States
• Hybrid · 2–3 days in office
• US$151,500 – US$252,500 pa
• Director

Leads cross-functional project teams within Oncology Translational Medicine, coordinating diagnostics, biomarker and clinical development activities with internal groups and external labs and manufacturers. Manages integrated timelines, budgets, contracts and invoices, tracks milestones and risks, and supports regulatory documentation and technical evaluations of diagnostic technologies.

Microsoft Project · Microsoft Word · Microsoft Excel +7

• USA - Pennsylvania - Upper Providence
• Hybrid · 2–3 days in office
• US$149,325 – US$248,875 pa
• Director

Leads epidemiology programs for one or more assets or disease areas, setting strategy and timelines with clinical development, safety, regulatory, outcomes and commercial partners. Designs, oversees and delivers observational and database studies using real-world data, registries and linked sources, and provides scientific advice on study design, analysis plans and interpretation. Manages external vendors, budgets and timelines, and prepares regulatory documents, technical reports and publications.

Electronic Health Records · Claims Data · Registries

• Waltham, United States
• Hybrid · 2–3 days in office
• US$149,325 – US$248,875 pa
• Director

Lead epidemiology programs for one or more assets or disease areas, setting strategy and timelines with clinical development, safety, regulatory, outcomes and commercial partners. Design, oversee and deliver observational and database studies using real-world data, registries and linked sources, while managing external vendors, budgets and timelines and preparing regulatory documents and publications.

Electronic Health Records · Claims Data · Registries

• London
• Hybrid · 2–3 days in office
• US$149,325 – US$248,875 pa
• Director

Leads epidemiology programs for one or more assets or disease areas, setting strategy and timelines with cross-functional partners. Designs, oversees and delivers observational and database studies using real-world data, registries and linked sources, and provides scientific advice on study design, data needs and analysis plans. Manages external vendors, budgets and timelines, and prepares regulatory documents, technical reports and publications.

Electronic Health Records · Claims Data · Registries

• USA - Pennsylvania - Upper Providence
• Hybrid · 2–3 days in office
• US$151,500 – US$252,500 pa
• Director

Leads cross-functional project teams within Oncology Translational Medicine to advance diagnostic and biomarker development programs, coordinating internal groups and external labs and Dx manufacturers. Manages integrated timelines, budgets, contracts and invoices, tracks milestones and risks, and supports regulatory documentation and technical evaluations. Hybrid role requiring 2-3 days per week onsite.

Microsoft Project · Microsoft Word · Microsoft Excel +7

• Rockville Tower Oaks Blvd
• Hybrid · 2–3 days in office
• US$149,325 – US$248,875 pa
• Director

Leads epidemiology programs for one or more assets or disease areas, setting strategy and timelines with clinical development, safety, regulatory, outcomes and commercial partners. Designs and delivers observational and database studies using real-world data, registries and linked sources, and provides scientific advice on study design, analysis plans and interpretation. Manages external vendors, budgets and timelines, and prepares regulatory documents, technical reports and publications.

Electronic Health Records · Claims Data · Registries +1

• Durham Blackwell Street
• Hybrid · 2–3 days in office
• US$149,325 – US$248,875 pa
• Director

Leads epidemiology programs for one or more assets or disease areas, setting strategy and timelines with clinical development, safety, regulatory, outcomes and commercial partners. Designs, oversees and delivers observational and database studies using real-world data, registries and linked sources, and provides scientific advice on study design, data needs and analysis plans. Also manages external vendors, budgets and timelines, and prepares regulatory documents, technical reports and publications.

• USA - Pennsylvania - Upper Providence
• US$139,425 – US$232,375 pa
• Director

Acts as the operational hub for oncology assets, owning the integrated project plan, budget and risk inputs while driving critical-path acceleration and governance decisions. Partners with project leads to navigate uncertainty, facilitate high-performing teams and embed consistent project management practices across the pipeline.

Planisware · MS Project

• Waltham, United States
• US$139,425 – US$232,375 pa
• Director

Acts as the operational 'COO' of a drug or vaccine asset, owning the single integrated project plan and partnering with project leads to steer strategy through complexity. Drives critical-path acceleration, risk management, governance preparation and cross-functional handoffs, with budget and resource forecasting using tools such as Planisware or MS Project.

Planisware · MS Project

• USA - Pennsylvania - Upper Providence
• Hybrid
• US$123,000 – US$205,000 pa
• Lead

Owns operational delivery of diagnostics across early and late-stage oncology trials, from biosample collection and clinical trial assays at reference and central labs to analysis-ready, audit-ready data. Works in a matrix with strategy, biomarker, clinical operations, data management, regulatory, quality and procurement teams, plus external CROs, labs and vendors, and mentors colleagues as a subject matter expert.

CRO · Central Labs · Reference Labs