Biotechnology Jobs

GSK · USA - Pennsylvania - Upper Providence · £174,750 – £291,250 pa

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.

GSK · Boston, United States · £174,750 – £320,375 pa

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.

GSK · London

Lead authoring and strategic planning of clinical and regulatory documents such as protocols, clinical study reports, briefing documents and CTD submission dossiers. Manage end-to-end writing projects, coordinating contributors, timelines and quality checks, and act as subject matter expert on medical writing standards and regulatory expectations while driving process improvement and audit readiness.

GSK · USA - Pennsylvania - Upper Providence

Lead programming activities for complex and pivotal clinical studies, developing, maintaining and validating analysis packages while ensuring compliance with Good Programming Practices and CDISC standards. Mentor junior programmers, support regulatory interactions with EMA and FDA, and bridge scientific requirements with technical solutions in an agile, squad-based global team.

GSK · London

Leads digital products for structured, collaborative and increasingly automated authoring of evidence and regulatory content across clinical, CMC, safety, regulatory and publications. Owns the roadmap, backlog and value case, shaping technical trade-offs with architects and engineers while embedding GxP, data-integrity and AI-governance requirements. Also mentors other Product Owners and manages strategic technology suppliers.

GSK · Stevenage

Individual-contributor alliance lead owning the relationship with an established central laboratory partner, balancing strategic direction with day-to-day governance and delivery oversight. Embeds a new operating model, monitors KPIs and study delivery, resolves escalations, and uses AI tools such as Claude to analyse large datasets and drive continuous improvement.

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

Owns the clinical strategy, scientific narrative and benefit-risk framework for a genitourinary oncology asset, acting as the senior clinical voice on the Medicine Development Team core quad. Leads governance and investment discussions, Health Authority interactions and evidence-generation strategy, while directing Senior Scientists who handle study-level delivery. Hybrid role with at least two days per week on-site.

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

Owns the clinical strategy, scientific narrative and benefit-risk framework for a genitourinary oncology asset, acting as the senior clinical voice on the Medicine Development Team core quad. Leads governance and health authority interactions while directing Senior Scientists who handle study-level delivery, and mentors clinical development talent.

GSK · Zug, Switzerland · US$242,250 – US$403,750 pa

Owns the clinical strategy, scientific narrative and benefit-risk framework for a genitourinary oncology asset, acting as the senior clinical authority on the Medicine Development Team core quad. Leads governance and investment discussions, Health Authority interactions and evidence-generation strategy, while mentoring clinical development talent and applying AI-enabled analytics to speed decision-making.

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

Owns the clinical strategy, scientific narrative and benefit-risk framework for a genitourinary oncology asset, acting as the senior clinical authority within the Medicine Development Team. Leads governance and investment discussions, health authority interactions and evidence-generation strategy, while mentoring clinical development talent and applying AI-enabled analytics to speed decision-making.

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

Leads end-to-end Model-Informed Drug Development and clinical pharmacology strategy across the drug development lifecycle, from first-in-human studies through filing and lifecycle management. Coordinates CPMS activities across assets, approves study designs and regulatory documents, and works with cross-functional partners in digital medicine, translational imaging and systems modelling. Based in the newly established Clinical Pharmacology and Quantitative Medicine organisation.

GSK · London · US$222,750 – US$371,250 pa

Leads end-to-end Model-Informed Drug Development and clinical pharmacology strategy across the drug development lifecycle, from first-in-human studies through filing and lifecycle management. Coordinates CPMS activities across assets, approves study designs and regulatory documents, and works with digital medicine, imaging, modelling and data science partners. Reports into the Respiratory, Immunology & Inflammation Research Unit.

GSK · Stevenage · US$222,750 – US$371,250 pa

Leads end-to-end Model-Informed Drug Development and clinical pharmacology strategy across the drug development lifecycle, from first-in-human studies through filing and lifecycle management. Coordinates CPMS activities across assets, approves study designs and regulatory documents, and works with digital medicine, translational imaging and modelling specialists. Based in Stevenage with a planned relocation to Cambridge, UK by early 2029.

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

Leads end-to-end Model-Informed Drug Development and clinical pharmacology strategy across the drug development lifecycle, from first-in-human studies through filing and lifecycle management. Coordinates CPMS activities across assets, approves study designs and regulatory documents, and partners with digital medicine, translational imaging, biostatistics and AI/ML teams. Reports into the Respiratory, Immunology & Inflammation Research Unit within the new Clinical Pharmacology and Quantitative Medicine organisation.

GSK · London

Embedded with chemical manufacturing teams, you take AI use cases from problem framing to working prototypes at days-to-weeks cadence, building in-silico process models, digital twins and optimization solutions. Work is AI-augmented, with coding agents handling routine development while you supply judgement, validation and model identification. Proven solutions are packaged for handoff to a solutions engineer for scale-up.