Biotechnology Jobs

GSK · USA - Pennsylvania - Upper Providence · US$222,750 – US$371,250 pa

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.

GSK · Waltham, United States · US$222,750 – US$371,250 pa

Serves as the physician on a clinical program team, leading medical monitoring, safety oversight and data interpretation for oncology and hematology studies. Partners with a Senior Scientist and cross-functional groups on protocol development, regulatory interactions and investigator engagement within a matrix team. May guide other physicians on complex multi-study programs.

GSK · London · £35,000 pa

Two-year graduate programme rotating through Global Clinical Study Delivery, acting as a Study Manager on Phase I–IV trials. You manage study execution in line with GCP, from start-up to close-out, tracking budgets and timelines, maintaining eTMF completeness and clinical trial management systems, and collaborating with Global Study Managers, Leads and Specialists plus external vendors.

GSK · Stevenage · US$242,250 – US$403,750 pa

Leads the global development of a medicine from clinical Proof of Concept to approval in first major markets, acting as single point of accountability. Builds and directs a matrixed Medicine Development Team spanning clinical, medical, commercial and manufacturing, driving strategy, governance and go/no-go decisions. Hybrid role with at least two days on-site per week.

GSK · London

Owns the product vision and roadmap for AI-enabled digital products that support structured, collaborative authoring of evidence and regulatory content across clinical, non-clinical, CMC, safety, regulatory and publications. Leads a multi-disciplinary product team, shapes scalable architecture with engineers, and drives an AI-first approach with GxP, privacy and AI governance embedded from the outset.

GSK · USA - Pennsylvania - Upper Providence · US$242,250 – US$403,750 pa

Leads the global development of a medicine from clinical Proof of Concept to approval in first major markets, acting as the single point of accountability. Builds and directs a matrixed Medicine Development Team spanning clinical, medical, commercial and manufacturing, and owns the asset budget and resourcing plan. Hybrid role requiring at least two days per week on-site at a US or UK GSK site.

GSK · Waltham, United States · US$242,250 – US$403,750 pa

Leads the global development of a medicine from clinical Proof of Concept through first major-market approval, acting as the single point of accountability. Builds and directs a matrixed Medicine Development Team spanning clinical, medical, commercial and manufacturing, and owns the asset's strategy, budget and governance decisions.

GSK · London · US$242,250 – US$403,750 pa

Leads the global development of a medicine from clinical Proof of Concept to approval in first major markets, acting as single point of accountability. Builds and directs a matrixed Medicine Development Team spanning clinical, medical, commercial and manufacturing, driving strategy, governance and go/no-go decisions. Hybrid role with at least two days per week on-site.

GSK · Stevenage

Manages statistical planning and delivery across oncology clinical programs, designing trials and analyses that shape development decisions and regulatory strategy. Works with clinical, regulatory, safety and clinical pharmacology teams, using simulation and advanced methods such as Bayesian and adaptive designs, while mentoring statisticians.

GSK · London

Manages statistical planning and delivery across oncology clinical programs, designing trials and analyses that shape development decisions and regulatory strategy. Works with clinical, regulatory, safety and clinical pharmacology teams, using simulation and advanced methods in R or Python, and mentors statisticians. Based in London or Stevenage, with a planned relocation to Cambridge by early 2029.

GSK · Stevenage

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.

GSK · UK - Hertfordshire - Ware RD

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.

GSK · Stevenage

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.

GSK · 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.

GSK · 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.