Biotechnology Jobs

• USA - Pennsylvania - Upper Providence
• On-site
• US$222,750 – US$371,250 pa
• Director

Serves as the physician within an oncology clinical programme team, leading medical monitoring and safety oversight for GI cancer studies. Interprets clinical and safety data, contributes to protocol development, and engages investigators, KEEs and health authorities. A core member of the Clinical Matrix Team, providing medical guidance within a matrixed pharma R&D environment.

AI-enabled insights

• London
• On-site
• US$242,550 – US$404,250 pa
• Director · manages people

Senior physician leader providing medical oversight, safety monitoring and clinical data interpretation across lung cancer studies within a clinical programme team. Partners with the Senior Scientist and cross-functional groups on protocol design, regulatory interactions and external scientific engagement, while mentoring Medical Directors. Requires an on-site presence at least two days a week.

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$340,500 – US$567,500 pa
• Director · manages people

Leads global development of a cancer vaccine asset from late-stage transition through approval and launch, acting as single point of accountability. Builds and directs a matrix Medicine Development Team spanning clinical development, immunology, manufacturing, regulatory, safety, medical affairs and commercial, and drives strategy, go/no-go decisions and lifecycle planning.

mRNA · Checkpoint Inhibitors

• Stevenage
• Lead

Designs, develops and maintains modular end-to-end data-flows across GSK's R&D ecosystem, turning scattered systems and sources into trusted, reusable, machine-readable assets. Embeds compliance-as-code and governance into pipelines, working with metadata ecosystems and agentic solutions on Azure or GCP, and coaches peers on data-flow best practice.

Azure · GCP

• UK - Hertfordshire - Ware RD
• On-site
• Lead
• Permanent

Designs and governs modular, end-to-end data-flows for GSK's R&D division, turning scattered systems into reusable, compliance-by-design assets in a machine-readable format. Involves translating business needs into technical data requirements, policy-as-code, metadata ecosystems and agentic solutions, with coaching and peer review across matrix teams.

Azure · GCP

• Stevenage
• On-site
• Mid-level
• Permanent

Designs, builds and maintains modular end-to-end data-flows across GSK's R&D division, integrating scattered systems and sources into reusable, machine-readable assets with compliance built into the pipeline. Combines hands-on coding and data specification work with coaching and peer review to raise the team's data-flow standards.

Azure · GCP

• 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

• London
• Hybrid
• Director

Leads the design and delivery of health economics and outcomes research evidence for a portfolio of HIV treatment and prevention medicines, spanning real-world evidence, clinical outcome assessments, evidence synthesis and economic modelling. Shapes integrated value evidence strategies with R&D, medical affairs, market access and external payers/HTA bodies, and sets patient-centred outcomes strategy across the portfolio.

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• £174,750 – £291,250 pa
• Director · manages people

Leads respiratory epidemiology and real-world evidence programs that inform vaccine development, accountable for at least one asset or disease area and its Global Epidemiology Plan. Designs and oversees complex observational studies using claims, EHR and registry data, advises clinical, safety and regulatory matrix teams, and manages external partnerships and scientific dissemination. Also mentors junior epidemiologists and represents the company with regulators and at international conferences.

Electronic Health Records · Claims Data · Registries

• Boston, United States
• Hybrid · 2 days in office
• £174,750 – £320,375 pa
• Director · manages people

Leads respiratory epidemiology and real-world evidence programs that inform vaccine development, designing and overseeing complex studies on disease burden, treatment patterns and safety. Partners across clinical development, safety, regulatory and health outcomes, manages external collaborations, and mentors junior scientists. Hybrid role requiring on-site presence at least two days per week.

• London
• Hybrid · 2 days in office
• £123,000 – £205,000 pa
• Director · manages people

Leads respiratory epidemiology and real-world evidence programmes that inform vaccine development, designing and overseeing complex studies on disease burden, treatment patterns and safety. Partners with clinical development, safety, regulatory and external collaborators, and mentors junior staff. Requires deep RWE and pharmaco-epidemiology expertise in a global, matrixed environment.

• Belgium-Wavre
• Hybrid · 2 days in office
• €123,000 – €205,000 pa
• Director · manages people

Leads respiratory epidemiology and real-world evidence programs that inform vaccine development, owning the epidemiology plan for at least one asset or disease area. Designs and oversees complex observational studies using claims, EHR and registry data, advises clinical, safety and regulatory teams, and manages external partnerships while mentoring junior scientists.

Electronic Health Records · Claims Data · Registries

• London
• Hybrid · 2–3 days in office
• Senior

Embedded forward deployed engineer role in GSK's Enterprise AI team, working within the Chemical Manufacturing & Control area to prototype AI solutions at days-to-weeks cadence. Focuses on document authoring and generation for regulatory filings, agentic workflows, RAG, knowledge systems and LLM evaluation, with heavy daily use of AI coding agents. Proven prototypes are handed off to a Sr. Solutions Engineer for scale-up.

Claude Code · GitHub Copilot · Databricks AI Assistant +3

• Stevenage
• Hybrid · 2–3 days in office
• Senior

Embedded with CMC business teams, you take high-priority AI use cases from problem framing to working prototypes at days-to-weeks cadence, then ship first production versions. The work centres on document authoring and generation for regulatory filings, building agentic and RAG pipelines, human-in-the-loop review workflows, and LLM evaluation with golden datasets and regression testing.

Claude Code · GitHub Copilot · Databricks AI Assistant +5