Latest Medical Services Jobs

Clinical Sciences Project Manager

This role involves managing and refining processes for investigator-sponsored research studies, supporting the Global Collaborative Studies Group in evidence generation, and leading the Request for Proposal study process. The candidate will work cross-functionally with various teams to ensure timely and compliant delivery of studies and contribute to the mission of advancing HIV research and treatment.

GSK United Kingdom

On-site Permanent

Clinical Sciences Project Manager

This role involves developing and refining processes, risk management strategies, and other activities essential to the success of the Global Collaborative Studies Group (CSG) at ViiV Healthcare. You will lead the Request for Proposal study process, manage study-related activities, and work cross-functionally with various teams to ensure timely and compliant delivery of supported studies.

GSK

On-site Permanent

Director, AI Engineering--Clinical Development and Operations (CD&O)

This role involves designing, building, and deploying production-grade AI systems to support clinical development and operations. You will develop and implement AI/ML models, automate manual processes, and create decision-support tools to improve operational efficiency. The role requires strong collaboration with cross-disciplinary teams and a focus on embedding MLOps best practices.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

Director, AI Engineering--Clinical Development and Operations (CD&O)

This role involves designing, building, and deploying production-grade AI systems to support clinical development and operations. You will develop and implement AI/ML models, automate manual processes, and create decision-support tools to improve operational efficiency. The role requires strong expertise in machine learning, software engineering, and cloud deployment, with a focus on practical, scalable solutions.

Pfizer

On-site Permanent

Regulatory Conformance Officer (12-month / Secondment)

As a Regulatory Conformance Officer, you will ensure that GSK's products meet all licensing and regulatory requirements, maintaining compliance with global market authorisations and supporting regulatory submissions. You will collaborate with multiple functions, including manufacturing, R&D, and global regulatory affairs, to deliver regulatory strategies and inspection readiness.

GSK Barnard Castle, United Kingdom

On-site Contract

Quality Validation and CSV Manager

The Quality Validation and CSV Manager will lead a team responsible for ensuring all validation activities, including process, cleaning, facility, and computer systems validation, comply with regulatory requirements and GSK quality standards. The role involves managing validation protocols, collaborating with cross-functional teams, and providing technical expertise and training.

GSK Barnard Castle, United Kingdom

On-site Permanent

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 strategies. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.

GSK Stevenage, United Kingdom

Hybrid Permanent

Director, QC Systems

This role involves leading a global matrix programme team to transform incoming material testing and data management across GSK's manufacturing sites. Responsibilities include defining future-state operating models, creating global standards, and ensuring harmonised QC master data structures while partnering with various teams to implement the strategy.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Director, QC Systems

This role involves leading a global matrix programme team to transform incoming material testing and data management across GSK's manufacturing sites. Responsibilities include defining future-state operating models, creating global standards, and ensuring harmonised QC master data structures while partnering with various teams to implement the strategy.

GSK Stevenage, United Kingdom

Hybrid Permanent

Head of Precision Diagnostics External Engagement

This senior role involves leading business development and transactions in biomarker and diagnostics for GSK's Oncology R&D. Responsibilities include negotiating deals, aligning with R&D strategy, and collaborating with internal and external stakeholders to drive strategic alliances and complex collaborations.

GSK Stevenage, United Kingdom £242,250 – £403,750 pa

On-site Permanent

Specialist - Extractables and Leachable - MSAT EM

This role involves leading Extractables and Leachables (E&L) assessments for biopharmaceutical manufacturing processes, container closure systems, and dosing devices. The Specialist will work with internal and external labs to ensure E&L testing is completed scientifically, compliantly, and cost-effectively, while also managing risk identification and escalation.

GSK East Hertfordshire, United Kingdom £70,650 – £117,750 pa

On-site Permanent

Protein Engineering and Innovation Scientist

This role involves leading the development and deployment of advanced in-silico protein engineering and design principles to generate complex reagents for drug discovery. You will collaborate with computational experts, protein expression teams, and external partners to design, generate, and test engineered proteins, contributing to scientific innovation and project delivery.

GSK Stevenage, United Kingdom

Hybrid Permanent

Director, Global Strategic Insights – Oncology

This role involves leading the generation of strategic insights for a key oncology brand within GSK's ADC portfolio. Responsibilities include shaping commercial forecasts, conducting global market research, and partnering with cross-functional teams to drive business strategy and competitive intelligence.

GSK

On-site Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of Biopharm, Vaccines, and Pharmaceutical facilities. You will evaluate compliance with GMP, policies, and regulatory requirements, and provide subject matter expertise on sterile manufacturing. The role requires strong communication and influencing skills, and involves travel to various sites across the network.

GSK East Hertfordshire, United Kingdom

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 the EMEA region. You will evaluate compliance with GMP, regulatory requirements, and quality management systems, and provide subject matter expertise in sterile manufacturing. The role requires strong communication and influencing skills to engage with senior stakeholders and produce clear audit reports.

GSK Worthing, United Kingdom

Hybrid Permanent