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Global Clinical Program lead

As a Clinical Program Lead, you will provide strategic leadership and scientific rigor for global evidence generation programs, ensuring diagnostic solutions are backed by robust data to improve patient outcomes. You will drive the development of Integrated Evidence Generation Plans and oversee the delivery of complex global clinical trials, collaborating with cross-functional teams to align strategic decisions and manage program risks.

Roche United States £100,000 – £150,000 pa

On-site Permanent

Global Clinical Program lead

As a Clinical Program Lead, you will provide strategic leadership and scientific rigor for global evidence generation programs, ensuring diagnostic solutions are backed by robust data. You will drive the development of Integrated Evidence Generation Plans and oversee complex global clinical trials, collaborating with cross-functional teams to align on strategic decisions and manage program risks.

Roche £80,000 – £120,000 pa

On-site Permanent

Senior Operating Partner, Drug Design, London

As a Senior Operating Partner in Drug Design, you will work closely with the Chief Scientific Officer and Chief Research Officer to drive high-priority initiatives, ensuring cross-functional collaboration and operational excellence. Your role involves synthesizing outputs, problem-solving, and facilitating the scaling of the organization's drug discovery efforts through strategic advice and hands-on execution.

Isomorphic Labs London, United Kingdom £80,000 – £120,000 pa

On-site Permanent

Global Clinical Program lead

As a Clinical Program Lead, you will provide strategic leadership and scientific rigor for global evidence generation programs, ensuring diagnostic solutions are backed by robust data. You will drive the development of Integrated Evidence Generation Plans and oversee complex global clinical trials, collaborating with cross-functional teams to achieve regulatory success and improve patient outcomes.

Roche £80,000 – £120,000 pa

On-site Permanent

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data generated for clinical-phase biomarker studies, ensuring accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve data discrepancies and maintain inspection readiness.

Moderna Oxford, United Kingdom £40,000 – £60,000 pa

On-site Temporary

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data generated for clinical-phase biomarker studies, ensuring data accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve discrepancies and maintain inspection readiness.

Moderna £40,000 – £60,000 pa

On-site Temporary

Sr. Manager, ICSR Quality

This role involves overseeing the quality and compliance of Individual Case Safety Reports (ICSRs) for multiple CSL products. Responsibilities include managing vendor relationships, ensuring consistent case processing, and contributing to ICSR quality strategy and reconciliation activities. The role requires strong pharmacovigilance experience and regulatory knowledge.

Appcast Enterprise Maidenhead, SL6 1QB, United Kingdom £40,000 – £60,000 pa

Hybrid Permanent

Principal Scientist, Genomics Analytics Engineer

This role involves designing and implementing maintainable analytics and ML pipelines for genomics and multi-omics data. You will translate scientific requirements into reliable software systems, own workflows from prototype to production, and act as a technical bridge between genomics scientists and AI/ML teams. The position emphasizes robustness, interpretability, and reproducibility in data analysis and machine learning.

GSK Stevenage, United Kingdom £80,000 – £120,000 pa

Hybrid Permanent

Project Engineer - Pharmaceutical Manufacturing

The Project Engineer will manage the end-to-end delivery of engineering projects in a highly regulated pharmaceutical manufacturing environment, including equipment installation, upgrades, and facility improvements. Key responsibilities involve supporting validation activities, troubleshooting new equipment, coordinating with internal and external teams, and implementing process improvements. Clean room experience is advantageous.

Smart4Sciences Guildford, Surrey, United Kingdom £50,000 pa

On-site Permanent

Project Manager - Pharmaceutical

This role involves managing the installation, commissioning, and validation of a pharmaceutical facility expansion. You will lead cross-functional teams, ensure compliance with quality and safety standards, and contribute to continuous improvement. The projects are complex and require a structured approach in a regulated environment.

Smart4Sciences Surrey, United Kingdom £50 – £55 ph

On-site Contract

Director, HTA, Value & Evidence (HV&E) - Obesity

This role involves leading the development and execution of global evidence generation strategies to support patient access to Pfizer’s Obesity treatments. The Director will manage health economics and outcomes research, coordinate with cross-functional teams, and develop strategic partnerships to ensure successful reimbursement and market access.

Pfizer £70,000 – £120,000 pa

Remote Permanent

Director, HTA, Value & Evidence (HV&E) - Obesity

The Director, HTA, Value & Evidence (HV&E) – Obesity will lead the development and execution of global evidence generation strategies to support patient access to Pfizer’s Obesity treatments. This involves managing health economics and outcomes research, coordinating with cross-functional teams, and developing strategic partnerships with external experts to ensure successful reimbursement and access requirements.

Pfizer United States £70,000 – £150,000 pa

On-site Permanent

Director, HTA, Value & Evidence (HV&E), Internal Medicine Early Pipeline

This role involves leading the development and execution of global evidence generation strategies to support patient access for Pfizer’s obesity and non-obesity products in early clinical development. The Director will work closely with cross-functional teams to design and conduct health economics and outcomes research (HEOR) studies, including real-world data studies and economic models, to inform healthcare decision-making and ensure successful market access and reimbursement.

Pfizer United States £120,000 – £180,000 pa

On-site Permanent

Director, HTA, Value & Evidence (HV&E), Internal Medicine Early Pipeline

This role involves leading the development and execution of evidence generation strategies to support patient access for Pfizer’s obesity and non-obesity products in early clinical development. The Director will work closely with cross-functional teams to design and conduct health economics and outcomes research (HEOR) studies, ensuring that the evidence aligns with global market access needs and regulatory requirements.

Pfizer £120,000 – £180,000 pa

Remote Permanent

Pharmaceutical Quality Engineer

The role involves providing quality engineering support across manufacturing, validation, and supply chain operations, ensuring compliance with GMP and GDP standards. Key responsibilities include leading deviation investigations, managing CAPA processes, and collaborating with cross-functional teams to drive continuous improvement in quality systems.

Smart4Sciences Cheshire, United Kingdom

On-site Contract Flexible