Latest Project Services Jobs

VP and Head of Operational Effectiveness

Leads operational effectiveness for clinical trial programs across GSK’s R&D organisation, driving process reimagination, performance intelligence, and transformation to accelerate drug development. Focuses on data-driven insights, operational excellence in third-party delivery and documentation, and capability building to improve speed, quality, and compliance in clinical operations.

GSK Stevenage, United Kingdom €190,500 – €317,500 pa

Hybrid Permanent

Regional Regulatory Manager

The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global goals and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, anticipating risks, and driving timely submissions and approvals.

GSK United Kingdom

Hybrid Permanent

Associate Director- Diagnostics Precision Medicine

This role involves leading diagnostic strategy and project execution in oncology translational medicine, supporting drug development through biomarker-driven clinical studies. The individual will oversee assay development and validation, ensure regulatory compliance, and collaborate across cross-functional teams and external partners. It emphasizes end-to-end ownership of diagnostic initiatives within a global biopharma R&D environment.

GSK £150,975 – £251,625 pa

Hybrid Permanent

SERM Scientific Director

The SERM Scientific Director at GSK leads the safety evaluation and risk management of oncology assets in clinical development. This role involves driving pharmacovigilance activities, evaluating safety data, and collaborating with cross-functional teams to ensure robust benefit-risk profiles and patient safety. The position requires significant experience in pharmacovigilance and a strong understanding of global regulations.

GSK

On-site Permanent

SERM Medical/Scientific Director

This role involves providing medical and scientific leadership in the safety evaluation and risk management of ViiV assets during clinical development. The individual will interpret safety data, identify and escalate safety signals, and deliver evidence-based recommendations to inform benefit-risk decisions. They will lead cross-functional teams, contribute to global regulatory submissions, and represent GSK in interactions with regulatory authorities, ensuring patient safety and shaping the safety profile of innovative specialty medicines.

GSK United Kingdom

Hybrid Permanent

ViiV Healthcare (GSK) Director, Scientific Communications and Medical Education

ViiV Healthcare is a global specialty HIV company, the only one that is 100% focused on researching and delivering new medicines for people living with, and at risk of, HIV. ViiV is highly mission-driven in our unrelenting commitment to being...

GSK United States

ViiV Healthcare (GSK) Director, Scientific Communications and Medical Education

ViiV Healthcare is a global specialty HIV company, the only one that is 100% focused on researching and delivering new medicines for people living with, and at risk of, HIV. ViiV is highly mission-driven in our unrelenting commitment to being...

GSK

Manager, Managed Access, Oncology

Manager, Managed Access, OncologyThis position will be offered on a 15-month contractLocation – GSK LondonJoin GSK's Medical Affairs team and be part of a global organization that drives innovation, scientific excellence, and patient-centered solutions. At GSK, we are committed to...

GSK United Kingdom

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with internal and external teams to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and supplies.

GSK Stevenage, United Kingdom

Hybrid Permanent

Senior Director, Translational Genetics

Leads a team of translational genetics scientists to drive data-driven insights in drug discovery and development, integrating genetic, genomic, and clinical data to address key translational questions across therapeutic areas. Focuses on target validation, biomarker discovery, and patient subgroup identification using advanced statistical genetics and analytical methods. Operates in a multidisciplinary environment, fostering innovation and external collaborations to accelerate the GSK pipeline.

GSK Stevenage, United Kingdom US$207,075 – US$345,125 pa

Hybrid Permanent

Senior Director, Translational Genetics

Leads a team of translational genetics scientists to integrate genetic, genomic, and clinical data in support of drug discovery and development. Focuses on generating disease-relevant insights using statistical genetics and multi-omics approaches across key therapeutic areas. Works within cross-functional teams and drives external collaborations to advance GSK’s R&D pipeline.

GSK Canterbury, United Kingdom US$207,075 – US$345,125 pa

Hybrid Permanent

Director, Translational Science Lead

This role leads translational science strategy across renal, inflammation, fibrosis, and neurodegeneration disease areas, driving biomarker development and validation to support clinical decision-making from preclinical through to launch. The position integrates cutting-edge technologies like spatial transcriptomics and human multi-omics data, working across discovery and development to de-risk clinical transitions and identify responder populations.

GSK Stevenage, United Kingdom US$178,200 – US$297,000 pa

Hybrid Permanent

Director, Translational Science Lead

Leads translational science strategy for renal, inflammation, fibrosis, and neurodegeneration programs, driving biomarker development and validation from preclinical to clinical stages. Focuses on integrating multi-omics data, human assays, and novel technologies to inform clinical decision-making and patient stratification. Works across discovery and development to advance differentiated therapeutics through cross-functional collaboration and external partnerships.

GSK Canterbury, United Kingdom £178,200 – £297,000 pa

Hybrid Permanent

CMC Leader (Director)

Leads end-to-end CMC strategy and execution for a pharmaceutical product from early development through commercialisation, including process development, regulatory filings, and lifecycle planning. Coordinates cross-functional global teams across R&D, supply chain, and regulatory to deliver clinical and commercial supply, ensuring technical transfer, quality compliance, and launch readiness. Focuses on complex modalities such as small molecules and oligonucleotides, with strong emphasis on regulatory strategy, risk management, and transition to commercial operations.

GSK Stevenage, United Kingdom

Hybrid Permanent

CMC Leader (Director)

Leads the development, industrialization, and lifecycle delivery of a physical medicine from early development through commercialization, ensuring seamless transition across stages. Coordinates cross-functional CMC and supply chain teams to deliver regulatory filings, process validation, and launch readiness, with a focus on complex products including small molecules and oligonucleotides. Drives strategic decision-making across R&D, manufacturing, and commercial functions to ensure timely, compliant, and scalable product supply.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent