Latest Human Resource Consulting Jobs

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Medical Director, Clinical Development, Immunology

We are seeking a Medical Director, Clinical Development, Immunology for a clinical program in food allergy. The Medical Director, Clinical Development, Immunology will support the Clinical Development Lead (CDL) and clinical team to plan and execute a clinical program, consisting...

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Senior Director / Director, Non-Clinical Safety Project Specialist

This role leads non-clinical safety strategy across drug discovery and development, integrating scientific data into project narratives and regulatory submissions. The specialist provides expert guidance on safety assessment, candidate selection, and regulatory interactions, while mentoring teams and shaping translational development plans to support clinical progression and regulatory approvals.

GSK Stevenage, United Kingdom US$224,400 – US$374,000 pa
Hybrid Permanent
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Assistant General Counsel - R&D

Lead legal support for GSK’s R&D discovery and translational platforms, advising on collaborations, data governance, regulatory compliance, and risk management. Partner with scientific and business leaders to enable technology-driven drug discovery and development, draft complex agreements, and provide strategic legal guidance in a global, science-led environment.

GSK United Kingdom
Hybrid Permanent
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Assistant General Counsel - R&D

Lead legal support for GSK’s R&D Technologies and Translational Sciences teams, advising on collaborations, data governance, and regulatory compliance in drug discovery and development. Provide strategic legal guidance on academic partnerships, data licensing, and sample management while working cross-functionally to mitigate risks and accelerate R&D. Matrix-manage legal colleagues and contribute to policy responses and training to strengthen legal awareness across science teams.

GSK
Hybrid Permanent
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Assistant General Counsel - R&D

This role involves providing strategic legal leadership for GSK’s R&D Technologies and Translational Sciences teams, focusing on discovery and translational research platforms. The lawyer will advise on collaborations, data governance, regulatory compliance, and complex agreements with academic and commercial partners, while supporting innovation in biopharma R&D. The position requires close partnership with cross-functional teams and occasional international travel.

GSK
Hybrid Permanent
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Principal Medical Writer

The Principal Medical Writer will lead the creation of high-quality clinical and regulatory documents, working closely with cross-functional teams to ensure scientific rigor and clear communication. This role involves strategic planning, project management, and translating complex data into clear narratives, with a focus on regulatory compliance and process improvement.

GSK United States
On-site Permanent
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Principal Medical Writer

The Principal Medical Writer will lead the creation of high-quality clinical and regulatory documents, working closely with cross-functional teams to ensure scientific rigor and compliance. This role involves strategic planning, project management, and translating complex data into clear narratives, with a focus on regulatory submissions and process improvements.

GSK
On-site Permanent
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Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for oncology clinical programs, working closely with cross-functional teams to design robust clinical trials and drive methodological innovation. You will mentor colleagues and contribute to regulatory strategy, using advanced statistical methods and simulations to inform trial design and risk assessment.

GSK
Hybrid Permanent
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Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategy. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.

GSK
Hybrid Permanent
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Principal Programmer / Analyst

This role involves leading programming activities for complex clinical studies, ensuring high-quality and timely outputs. You will collaborate with cross-functional teams, mentor junior programmers, and support regulatory interactions, while fostering quality assurance and innovation.

GSK
Hybrid Permanent
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Therapy Supply Chain Manager

Leads end-to-end supply planning and execution for a designated therapy area, ensuring uninterrupted patient access to medicines. Works cross-functionally across planning, manufacturing, quality, and commercial teams to resolve supply disruptions, drive inventory optimisation, and implement continuous improvement initiatives using data analysis and planning systems. Focuses on risk mitigation, regulatory compliance, and performance monitoring within a global pharmaceutical supply chain.

GSK United Kingdom
Hybrid Temporary
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Project Specialist (External Manufacturing-Drug Product)

This role involves managing technology transfer projects for external drug product manufacturing, coordinating between GSK and Contract Manufacturing Organisations (CMOs) to ensure timely and compliant delivery. The specialist will drive project schedules, mitigate risks, align cross-functional teams, and maintain governance across the supply chain, particularly for sterile drug products like monoclonal antibodies and vaccines. A key focus is ensuring technical knowledge retention and operational readiness for new suppliers or assets.

GSK United Kingdom €69,600 – €116,000 pa
Hybrid Permanent
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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
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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
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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