Latest Professional Services Jobs

Manager, Labelling Strategy and Development

This role involves leading the development and maintenance of global product labelling, including prescribing information and patient leaflets, for pharmaceutical products. The manager will collaborate with cross-functional teams to ensure accurate, compliant, and scientifically sound labelling across international markets, supporting medicines throughout their lifecycle. Key responsibilities include authoring regulatory documents, aligning labelling strategy, and mentoring team members within a global regulatory environment.

GSK United Kingdom

Hybrid Permanent

MSAT Molecule Steward

This role involves providing end-to-end technical leadership for a pharmaceutical product throughout its lifecycle, from development through manufacturing and commercial supply. The Molecule Steward ensures product quality, process robustness, and regulatory compliance by leading technical strategy, coordinating cross-functional teams, and driving continuous improvement across global supply chain sites. The position requires deep scientific expertise, strong leadership in matrixed environments, and active involvement in regulatory submissions and lifecycle management.

GSK €103,500 – €172,500 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role leads operational excellence for Supported Studies at GSK, focusing on data integrity, system governance, and digital transformation. The individual will own the data and dashboard ecosystem, act as Business System Owner for key platforms like IdeaPoint and Veeva, and ensure compliance with regulatory requirements such as Transfer of Value. They will bridge business and technology to drive process improvements, enable resource planning, and enhance data transparency across clinical operations.

GSK £154,275 – £257,125 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role focuses on strengthening the operational and digital foundations of GSK's Supported Studies program. The Associate Director will lead data governance, system ownership, and digital integration efforts, ensuring data integrity, compliance, and efficiency across platforms like Veeva and IdeaPoint. The position acts as a bridge between business and technology, driving process improvements and digital transformation in a regulated clinical environment.

GSK US$154,275 – US$257,125 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role leads the operational and digital foundations for Supported Studies at GSK, ensuring data integrity, system performance, and compliance across platforms like Veeva and IdeaPoint. The individual will drive process improvements, support regulatory reporting such as Transfer of Value, and act as a bridge between business and technology teams to enhance efficiency and scalability in clinical operations.

GSK US$154,275 – US$257,125 pa

Hybrid Permanent

Project Specialist (External Manufacturing-Drug Product)

The role involves managing technology transfer projects for external manufacturing of drug products, coordinating between GSK and Contract Manufacturing Organisations (CMOs). The specialist ensures timely delivery of critical path activities, aligns internal and external stakeholders, and maintains governance across procurement, quality, technical, and supply functions, particularly for sterile drug products like monoclonal antibodies and vaccines.

GSK €69,600 – €116,000 pa

Hybrid Permanent

ViiV Healthcare (GSK) Director, Clinical Pharmacology

This role involves leading clinical pharmacology strategy across HIV drug development programs, applying PK/PD and pharmacometric modeling to inform study design, regulatory decisions, and development pathways. The Director will mentor project leads, collaborate with cross-functional teams, and serve as a scientific expert in modeling and simulation to advance ViiV’s mission-driven HIV research from early to late-stage development.

GSK United States

Hybrid Permanent

ViiV Healthcare (GSK) Director, Clinical Pharmacology

This role involves providing scientific leadership in clinical pharmacology to shape drug development programs for HIV treatments. The Director will apply PK/PD, pharmacometrics, and model-informed drug development approaches to guide study design, regulatory strategy, and key decisions across early to late-stage development. Collaboration with cross-functional teams including clinical, regulatory, biostatistics, and CMC is central to advancing innovative therapies in a mission-driven environment focused on eradicating HIV.

GSK

Hybrid Permanent

ViiV Healthcare (GSK) Director, Clinical Pharmacology

This role involves leading clinical pharmacology strategy across HIV drug development programs, applying PK/PD, pharmacometrics, and modeling to inform study design, regulatory decisions, and development pathways. The Director will mentor project leads, collaborate with cross-functional teams, and serve as a scientific expert in model-informed drug development, contributing to breakthroughs in HIV treatment and prevention.

GSK

Hybrid Permanent

Executive Director, Oncology Search & Evaluation

This role leads oncology business development and licensing initiatives at GSK, focusing on identifying and evaluating external innovation opportunities. The Executive Director will conduct scientific and strategic due diligence, build partnerships with biotech firms, and present investment cases to senior leadership, playing a central role in shaping GSK’s oncology pipeline.

GSK United States US$229,350 – US$382,250 pa

Hybrid Permanent

Executive Director, Oncology Search & Evaluation

This role involves leading oncology business development and licensing initiatives at GSK by identifying and evaluating external innovation opportunities. The Executive Director will lead due diligence, build strategic partnerships with biotech firms, and present investment recommendations to senior leadership. It requires deep scientific expertise, deal-making experience, and the ability to navigate complex cross-functional environments to advance GSK’s oncology pipeline.

GSK £229,350 – £382,250 pa

Hybrid Permanent

Senior Director RIIRU & TDS Strategy

This role leads high-impact strategic initiatives within GSK’s Respiratory Immunology and Inflammation Research Unit and Translational and Development Sciences organisation. The Senior Director will shape asset and portfolio strategy, interpret clinical and external data to inform investment decisions, and support governance processes at the R&D Leadership and Executive Committee levels. The position acts as a key interface with external partners and drives priority technology programmes while mentoring junior team members.

GSK United Kingdom

Hybrid Permanent

Senior Director / Director, Non-Clinical Safety Project Specialist

This role leads non-clinical safety strategy across drug discovery and development, integrating scientific data to inform project decisions, regulatory submissions, and risk assessment. The specialist provides expert guidance on safety profiling, candidate selection, and translational planning, while mentoring teams and shaping regulatory narratives. They work cross-functionally to ensure robust safety evaluation for small molecules and biologics through clinical and post-market stages.

GSK £224,400 – £374,000 pa

On-site Permanent

Senior Director / Director, Non-Clinical Safety Project Specialist

This role leads non-clinical safety strategy across drug discovery and development, integrating scientific data to inform project decisions, regulatory submissions, and risk assessment. The position involves mentoring teams, shaping translational plans, and providing expert input on safety profiling and candidate selection. It plays a key part in regulatory strategy and cross-functional leadership within a global biopharma environment.

GSK £224,400 – £374,000 pa

Hybrid Permanent

Director, Global RWE-HO, Oncology

Leads the planning, design, and execution of real-world evidence (RWE) and health outcomes studies to support oncology assets across the product lifecycle. Collaborates with cross-functional teams to generate robust evidence for regulatory, reimbursement, and market access decisions. Focuses on translating clinical and economic value into impactful data for payers, providers, and patients.

GSK United States

Hybrid Permanent