Latest Human Resource Consulting Jobs

ViiV Healthcare (GSK) Medical Director, ViiV R&D Physician Center of Excellence

This Medical Director role involves managing and overseeing Phase 1-4 clinical trials for ViiV Healthcare, focusing on the development of innovative HIV treatments. Key responsibilities include designing study protocols, ensuring medical governance, managing safety events, and collaborating with internal and external stakeholders to drive the success of clinical trials.

GSK

On-site Permanent

ViiV Healthcare (GSK) Medical Director, ViiV R&D Physician Center of Excellence

The Medical Director role at ViiV Healthcare focuses on managing and overseeing Phase 1-4 clinical trials, ensuring the successful planning, execution, and reporting of protocols. Key responsibilities include providing medical governance, managing safety events, and collaborating with internal and external stakeholders to develop groundbreaking HIV treatments.

GSK

On-site 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

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

Team Lead, Therapeutic Area Quality

This role involves leading a team of Quality Business Partners to ensure quality is integrated into R&D programs and projects. Responsibilities include evaluating quality strategies, driving continuous improvements, and supporting health authority inspections. The role also focuses on talent development and maintaining expertise in international regulations.

GSK

On-site Permanent

Team Lead, Therapeutic Area Quality

This role involves leading a team of Quality Business Partners to ensure quality is integrated into R&D programs and projects. Responsibilities include driving quality improvements, supporting health authority inspections, and contributing to the quality strategy and risk management. The role requires a deep understanding of regulatory requirements and the ability to lead a global quality team.

GSK

On-site 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

Manager, Translational Biomarker Data Pathways & Re-use

This role involves leading the setup, stabilization, and scaling of end-to-end translational data pathways, ensuring biomarker datasets are reusable and accessible. Key responsibilities include resolving systemic barriers, aligning data delivery with decision timelines, and developing repeatable processes for data re-use across multiple functions.

GSK Stevenage, United Kingdom

Hybrid Permanent

Manager, Labelling Strategy and Development

Lead the development and maintenance of global product labelling, including datasheets, prescribing information, and patient leaflets, ensuring accurate scientific and medical content across international markets. Collaborate with cross-functional teams in regulatory, clinical, safety, and governance to support product lifecycle management and compliance. Mentor team members, maintain documentation in regulatory systems, and contribute to labelling strategy in a complex global environment.

GSK Stevenage, United Kingdom

Hybrid Permanent

Small Molecule CMC Leader - Senior Director

Leads Chemistry, Manufacturing and Controls (CMC) strategy and execution for small molecule, biopharm, or cell and gene therapy medicines from late-stage development through commercialisation. Oversees process development, regulatory filings, supply chain, and lifecycle management across global teams and external partners, ensuring readiness for approval and launch. Role involves high-level governance engagement, risk management, and transition to commercial supply.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Executive Director, External Strategy & Science Advocacy

This role involves leading the external engagement and policy advocacy for GSK's Development Sciences, working with regulatory bodies, industry consortia, and academic institutions to shape the future of pharmaceutical innovation. Key responsibilities include developing policy strategies, advancing technical capabilities, and building strategic partnerships.

GSK United States

On-site Permanent

Executive Director, External Strategy & Science Advocacy

This role involves leading the external engagement and policy advocacy for GSK's Development Sciences, working closely with regulatory agencies, industry consortia, and government bodies to shape the future of pharmaceutical innovation. The Executive Director will drive strategic partnerships, develop policy frameworks, and champion technical advancements in clinical development and data science.

GSK

On-site Permanent

Executive Director, External Strategy & Science Advocacy

This role involves leading the external engagement and policy advocacy for GSK's Development Sciences, working closely with regulatory agencies, industry consortia, and academic institutions to shape the future of pharmaceutical innovation. Key responsibilities include developing policy strategies, advancing technical capabilities, and fostering strategic partnerships.

GSK

On-site Permanent