Latest Recruitment Jobs

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology portfolio, focusing on advancing the development of antibody drug conjugates (ADCs) for solid tumors. Key responsibilities include collaborating with multidisciplinary teams to design and execute clinical trials, ensuring high-quality protocol development, and engaging with key external experts to drive data generation and regulatory approvals.

GSK

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the clinical research activities for GSK’s oncology portfolio, including developing and executing phase 1-3 clinical trials. They will collaborate with various stakeholders to ensure high-quality protocol development, medical monitoring, and data interpretation, while also engaging with key external experts and thought leaders.

GSK

Hybrid Permanent

Clinical Data Analyst – Evinova

The Clinical Data Analyst role involves managing and optimizing clinical trial data, collaborating with cross-functional teams, and contributing to the development of data products. Responsibilities include data management, standards validation, pipeline configuration, troubleshooting, and continuous process improvement.

AstraZeneca London, United Kingdom

On-site Permanent

Automation/Process Control Engineer

This role involves strengthening control systems in AstraZeneca's manufacturing network, using digitalization and Lean techniques to improve production speed, resilience, and quality. The engineer will manage small projects, provide technical support, and mentor peers in automation and control systems.

AstraZeneca Macclesfield, United Kingdom

On-site Contract

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across EMEA and other highly regulated markets. Responsibilities include evaluating compliance, conducting various types of audits, and producing clear audit reports to inform senior management of identified risks and corrective actions.

GSK

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across EMEA and other highly regulated markets. You will evaluate compliance with GMP, regulatory requirements, and quality systems, and provide sterile manufacturing expertise. The role requires strong communication and stakeholder engagement skills.

GSK

Hybrid Permanent

Senior Director Translational Data Sciences

This role involves developing and executing a translational data strategy that bridges the gap between disease biology and clinical outcomes. The Senior Director will lead a team in integrating multi-omics data with AI-driven analytics, forming strategic partnerships, and ensuring clinical relevance in all analytical platforms.

GSK

On-site Permanent

Senior Director Translational Data Sciences

This role involves developing and executing a translational data strategy that bridges the gap between disease biology and clinical outcomes. The Senior Director will lead a team in integrating multi-omics data with AI-driven analytics, collaborate with R&D and clinical development, and establish high-value partnerships with external organizations.

GSK

On-site Permanent

Pharmacovigilance Quality Assurance Director

This senior role involves leading and maintaining a robust pharmacovigilance quality assurance programme, ensuring compliance with global regulations and internal standards. Key responsibilities include overseeing PV processes, managing audits, and providing strategic guidance to ensure patient safety and continuous improvement.

GSK United Kingdom

Hybrid Permanent

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

Leads clinical operations strategy and delivery across Hepatology, Renal, and Cardiovascular disease portfolios, managing a matrix team to ensure high-quality, on-time execution from early phase through lifecycle management. Drives data-informed decision-making, risk mitigation, and innovation adoption while aligning with enterprise goals and regulatory standards.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMOs, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK Irvine, Alba / Scotland, KA12 8EL, United Kingdom

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMOs, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK

Hybrid Permanent

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

Lead clinical operations strategy for Hepatology, Renal, and Cardiovascular disease portfolios within GSK's R&D engine. Drive end-to-end delivery of global clinical assets, manage high-performing teams, and ensure operational excellence across phases I–IV. Champion data-driven decision-making, inspection readiness, and innovation while aligning with enterprise goals and shaping future development operations.

GSK United Kingdom US$242,550 – US$404,250 pa

Hybrid Permanent