Latest Healthcare Jobs

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

RTSM Project Manager

The RTSM Project Manager is responsible for the design, development, testing, and maintenance of clinical studies using the RAMOS IRT system. Key responsibilities include ensuring data integrity, configuring complex study designs, and driving continuous improvements in clinical supplies systems. The role involves technical oversight, problem-solving, and collaboration with cross-functional teams to enhance IRT processes and support clinical development.

GSK Stevenage, United Kingdom

Hybrid Permanent

Field Service Engineer (Omagh, Enniskillen, border regions)

This role involves providing frontline technical support for Roche's diagnostic products in the Omagh, Enniskillen, and border regions. Responsibilities include troubleshooting, preventative maintenance, technical training, and ensuring regulatory compliance. The position emphasizes customer satisfaction and continuous improvement.

Roche United Kingdom

On-site Permanent

Field Service Engineer (Omagh, Enniskillen, border regions)

This role involves providing frontline technical support for Roche's diagnostic products in the Omagh, Enniskillen, and border regions. Responsibilities include troubleshooting, preventative maintenance, technical training, and ensuring regulatory compliance. The position requires a strong technical background and the ability to work effectively in a fast-paced, customer-focused environment.

Roche

On-site Permanent

Clinical Development Director - Renal

The Clinical Development Director is responsible for leading and supporting the delivery of clinical deliverables for a section of a global clinical program or a large, complex trial. This role involves collaborating with various teams to ensure data quality, regulatory compliance, and scientific accuracy in clinical trials and publications.

Novartis London, United Kingdom

Hybrid Permanent

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

The Data QC Specialist will perform detailed quality control reviews of laboratory data and documentation to ensure 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

On-site Temporary

Senior Systems Engineer, GXP Systems

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna Oxford, United Kingdom

On-site Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works across cross-functional teams to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a complex, global environment.

GSK United States US$144,375 – US$240,625 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Lead CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Work cross-functionally to ensure compliance, support inspections, and maintain product supply. Influence regulatory decisions and mentor teams within a complex, matrixed environment.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works across cross-functional teams to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a complex, global environment.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and ensuring compliance with global regulations. Works cross-functionally to address complex CMC issues, support inspections, and influence regulatory decisions. Focuses on maintaining product supply and optimizing regulatory processes across international markets.

GSK £144,375 – £240,625 pa

Hybrid Permanent