Latest Professional Services Jobs

Team Lead, Therapeutic Area Quality

The Team Lead, Therapeutic Area Quality, leads a team of Quality Business Partners, ensuring quality is integrated into R&D programs and projects. Key responsibilities include driving quality improvements, supporting health authority inspections, and contributing to the quality strategy and risk management.

GSK United Kingdom

On-site Permanent

Team Lead, Therapeutic Area Quality

The Team Lead, Therapeutic Area Quality, leads a team of Quality Business Partners, ensuring quality is integrated into R&D programs and projects. Responsibilities include driving quality improvements, supporting health authority inspections, and contributing to the global audit plan. The role also involves talent development and maintaining expertise in international regulations.

GSK

On-site Permanent

Senior Director Translational Data Sciences

This role involves developing and executing a translational data strategy that bridges the gap between disease biology and clinical outcomes. The Senior Director will lead a team in integrating multi-omics data with AI-driven analytics, forming strategic partnerships, and ensuring clinical relevance in all analytical platforms.

GSK Stevenage, United Kingdom

On-site Permanent

Principal Scientist, Innovation ETCT

The Principal Scientist role involves leading target discovery and early biologics programs, specifically focusing on antibody drug conjugates (ADCs) and T cell engaging bispecific antibodies (TCEs). You will collaborate with internal and external teams to accelerate the development of next-generation biologics for cancer therapy, contributing to the preclinical development of novel biologics.

GSK Stevenage, United Kingdom

Hybrid Permanent

Principal Scientist

This role involves leveraging cutting-edge computational approaches to understand and treat cancer. You will analyze and integrate multi-omics and clinical data to characterize disease heterogeneity, model disease evolution, and investigate treatment response. Collaboration with experimental and clinical teams is key to translating complex data into actionable insights for drug discovery.

GSK Stevenage, United Kingdom

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects from internal and external donor sites to external Contract Manufacturing Organizations (CMOs). Key responsibilities include managing project schedules, mitigating risks, and ensuring timely delivery within budget, while acting as the main point of contact between GSK and suppliers.

GSK Montrose, Alba / Scotland, DD10 8JB, United Kingdom

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK Worthing, United Kingdom

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

Leads clinical operations strategy and delivery across Hepatology, Renal, and Cardiovascular disease portfolios within GSK’s R&D engine. Oversees end-to-end development from early phase through life-cycle management, driving operational excellence, team development, and cross-functional alignment. Champions data-driven decision-making, risk management, and innovation adoption to accelerate high-impact assets.

GSK Stevenage, United Kingdom US$242,550 – US$404,250 pa

Hybrid Permanent

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

Lead clinical operations strategy for Hepatology, Renal, and Cardiovascular disease portfolios, driving end-to-end delivery from early phase through life-cycle management. Oversee a matrix team, align operational execution with R&D goals, and champion data-driven decision-making and innovation in clinical development. Shape culture, manage risks, and ensure inspection readiness across global assets.

GSK Canterbury, United Kingdom US$242,550 – US$404,250 pa

On-site Permanent

Statistics Director, Oncology

This role involves leading statistical strategies for key oncology programs, designing robust clinical trials, and mentoring statisticians. The position emphasizes innovation, regulatory interactions, and cross-functional collaboration to advance the development of new cancer therapies.

GSK Stevenage, United Kingdom

On-site Permanent

Process Engineer

The Process Engineer role involves providing technical expertise to support safe and efficient manufacturing at GSK's Montrose site. Responsibilities include resolving technical issues, contributing to capital projects, improving process plant software, and collaborating with cross-functional teams to ensure compliance and process improvements.

GSK Montrose, Alba / Scotland, DD10 8JB, United Kingdom

On-site Contract

Operational Quality Director

The Operational Quality Director at GSK will lead the end-to-end quality oversight of manufacturing activities, ensuring compliance with GMP standards and regulatory requirements. Key responsibilities include managing batch documentation, overseeing real-time quality control, and leading the QP team to maintain high-quality standards and inspection readiness.

GSK East Hertfordshire, United Kingdom

On-site Permanent

Clinical Programmer/Analyst

The Clinical Programmer/Analyst designs, builds, and reviews programming solutions to transform clinical and real-world data into reliable results for regulatory and research purposes. Working closely with statisticians and data scientists, the role involves developing validated datasets, tables, listings, and figures using CDISC standards such as SDTM and ADaM, while ensuring compliance with GxP and ICH guidelines. The position supports agile delivery within a hybrid work environment and emphasizes technical excellence, collaboration, and innovation in clinical data programming.

GSK Stevenage, United Kingdom

Hybrid Permanent