Latest Human Resource Consulting Jobs

Director, Oncology Clinical Biomarkers

This role involves developing and implementing biomarker strategies to support the clinical development of late-stage oncology assets. Responsibilities include collaborating with cross-functional teams, validating biomarker strategies, and integrating these into clinical plans to optimize decision-making and patient stratification.

GSK £189,750 – £316,250 pa

On-site Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK’s global assets, with a focus on safety evaluation in clinical development and post-marketing settings. The Scientific Director will lead cross-functional teams, drive safety governance, and ensure regulatory compliance across international markets. The position requires deep expertise in drug safety, signal detection, and benefit-risk assessment to protect patient safety and support regulatory submissions.

GSK United States US$169,950 – US$283,250 pa

On-site 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

NIS P&D Study Delivery Lead, Associate Director

The NIS P&D Study Delivery Lead, Associate Director, is responsible for leading the full lifecycle of clinical studies and trials within the Non-Interventional Study (NIS) portfolio. This includes designing, executing, and reporting complex regulatory commitment studies, managing team members, and ensuring compliance with regulatory guidelines. The role also involves leading operational decision-making, risk management, and driving innovation in study delivery through new technologies.

GSK Stevenage, United Kingdom £87,000 pa

Hybrid Permanent

Director, CMC Regulatory Affairs

Leads global CMC regulatory strategy for small molecule medicines, shaping development and approval pathways across international markets. Works at the intersection of R&D, supply, quality, and commercial functions to ensure regulatory compliance and uninterrupted patient access. Focuses on solving complex regulatory challenges, mentoring talent, and improving processes to support long-term product success.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

NPI Launch Lead

This role leads the logistics and project management for new pharmaceutical and consumer product launches at GSK’s Barnard Castle site, ensuring timely, compliant market rollouts. The NPI Launch Lead coordinates cross-functional teams, manages launch timelines across global markets, and ensures adherence to GMP, quality, and regulatory standards throughout the product introduction lifecycle.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Steriles Operator - Multiple Positions Available

This role involves operating and monitoring semi-automatic and fully automatic packaging, assembly, and inspection equipment in a sterile manufacturing environment. You'll ensure product quality through visual inspections, maintain accurate batch documentation in compliance with GMP standards, and support the production of medicines and vaccines in a regulated, classified environment. The position requires working closely with cross-functional teams to resolve discrepancies and maintain efficient, compliant operations.

GSK Barnard Castle, United Kingdom

On-site Permanent

Process Technologist

As a Process Technologist, you will support the production area by providing technical services, troubleshooting, and working on technical projects. You will collaborate with cross-functional teams to ensure product quality and compliance, execute process validation, and perform root cause analysis for material and processing issues.

GSK Barnard Castle, United Kingdom

On-site Permanent

Laboratory Analyst

The Laboratory Analyst supports product testing and analysis within GMP-compliant laboratories at GSK’s Ware site, ensuring safe and effective oral and solid dose medicines are produced. The role involves sample preparation, analytical testing using methodologies like HPLC, and maintaining compliance with safety and quality standards. Collaboration with cross-functional teams is key to maintaining supply and driving continuous improvement in a fast-paced manufacturing environment.

GSK East Hertfordshire, United Kingdom

On-site Permanent

Principal Programmer / Analyst

The Principal Programmer / Analyst 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 innovation and quality assurance in a global, agile environment.

GSK Stevenage, United Kingdom

Hybrid Permanent

Scientist, Analytical Operations - Small Molecule Stability Data Management

This role involves managing and improving stability data for small molecule studies, creating and maintaining study protocols, and producing clear data visualizations for regulatory submissions. You will work closely with cross-functional teams and external partners to drive process improvements and ensure data integrity.

GSK Stevenage, United Kingdom

Hybrid Permanent