Biotechnology Jobs

• Oxford
• Hybrid
• Permanent

The role sits within a mission-driven institute translating scientific discovery into real-world impact across health, generative biology, food security, climate and AI. Day-to-day work centres on computational biology research, collaborating with scientists, technologists and policy makers in an interdisciplinary environment.

• Oxford
• Hybrid
• Senior
• Permanent

Builds and operates high-performance GPU training and inference clusters, focusing on scheduling, isolation and automated lifecycle management. Optimises high-throughput data paths, I/O, caching and Lustre storage, and profiles bottlenecks across compute, network and orchestration layers. Works with research and data teams on capacity planning, quotas and ML experimentation pipelines.

Lustre

• Zug, Switzerland
• Hybrid · 2–3 days in office
• US$222,750 – US$371,250 pa
• Director

Serves as the physician within a clinical programme team, leading medical monitoring, safety oversight and data interpretation for GI oncology studies. Partners with a Senior Scientist and cross-functional matrix teams on protocol development, regulatory interactions and investigator engagement. Requires an on-site presence 2-3 days a week across UK, Swiss or US sites.

AI-enabled Insights

• Durham, United States
• US$148,500 – US$336,875 pa
• Director

Drives the development and execution of the analytical network strategy across GSK's global supply chain, defining QC testing network principles and translating them into an operational roadmap. Partners with GSC Quality, MSAT, R&D and governance forums on NPI and commercial supply decisions, with a focus on large molecules, ADCs and oligonucleotides. Establishes KPIs and reporting to track strategy impact and mitigate network risk.

• London
• Hybrid
• Director

Lead statistical planning and delivery across oncology clinical programs, designing trials and analyses that shape development and regulatory strategy. Work with clinical, regulatory, safety, data science and commercial teams, using Bayesian methods and simulation in R or Python, while mentoring statisticians.

R · Python

• London
• Hybrid
• Lead

Lead complex oncology projects, designing and interpreting scientific and clinical strategies while guiding cross-functional teams on technical and regulatory matters. The role combines hands-on project leadership with mentoring colleagues and driving new methodologies, in a hybrid setup spanning London and Upper Providence.

• 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

• 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.

• London

Hands-on role designing, building and maintaining modular end-to-end data-flows across GSK's R&D division, integrating diverse sources into reusable, machine-readable assets with compliance built into the pipeline. Combines technical delivery and coding with coaching and peer review to embed industry best practice, working in a complex matrix environment with varied stakeholders.

Azure · GCP

• UK - Hertfordshire - Ware RD

Designs, builds and maintains modular end-to-end data-flows across GSK's R&D division, integrating diverse sources such as protocol development, DSUR and clinical trial data into a unified machine-readable format. Combines hands-on coding and orchestration with compliance-by-design, documentation and coaching or peer review to embed industry best practice.

Azure · GCP

• USA - Pennsylvania - Upper Providence
• Director

Accountable for GSK R&D's enterprise portfolio of external scientific content and data licenses, including budget, forecasting, cost controls and retiring under-used sources. Manages vendor relationships and commercial terms, maintains copyright-compliant governance and user guidance, and works across scientific, procurement, legal, digital and technology teams to make licensed content AI- and text-mining-ready.

Excel · PowerPoint · Word +2

• USA - Pennsylvania - Upper Providence
• Hybrid
• Director

Lead statistical planning and delivery across oncology clinical programs, designing trials and analyses that shape development and regulatory strategy. Work with clinical, regulatory, safety, data science and commercial teams, applying Bayesian methods, simulations and advanced modelling in R or Python, while mentoring statisticians.

R · Python