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On-site Permanent

Senior Bioinformatics Developer - Synthetic Biology

This role involves developing complex bioinformatic algorithms to categorize large datasets, designing sequencing tools, and integrating with lab systems. You will work in a multidisciplinary team of scientists and engineers, leading bioinformatics projects and contributing to cloud-based workflows for research teams.

Newton Colmore

Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Associate Director, Safety Epidemiology – Global Patient Safety

This role involves leading the design, execution, and reporting of post-authorisation safety studies using real-world data. The candidate will collaborate with various teams to produce high-quality evidence for regulatory decisions and risk management, ensuring AstraZeneca's medicines are safe and effective.

AstraZeneca

Chatham, ME4 4NP, United Kingdom

On-site Permanent

Associate Engineer, GxP IT Support

This role involves providing hands-on IT support for Moderna’s GMP manufacturing operations at the Harwell site. Key responsibilities include ensuring GMP compliance, triaging IT incidents, managing infrastructure, and collaborating with various teams to maintain robust and compliant systems. The position offers exposure to modern observability and cybersecurity tools, making it a dynamic opportunity for someone who thrives in complex, regulated environments.

Moderna

Oxford, United Kingdom

£189,750 – £316,250 pa On-site Permanent

Director, Oncology Clinical Biomarkers

This role involves developing and implementing biomarker strategies for late-stage oncology clinical trials, collaborating with cross-functional teams to identify patient populations and optimize drug development. The Director will leverage cutting-edge technologies and methodologies to validate biomarkers and inform clinical decisions.

GSK

Stevenage, United Kingdom

On-site Permanent

Senior Director Global Clinical Program Lead Cardiovascular & Renal

This role involves leading the clinical development and strategic oversight of a medicine for cardiovascular and renal conditions. Responsibilities include managing the Clinical Development Team, ensuring high clinical and scientific standards, and authoring key study documents and regulatory submissions.

CSL

Hybrid Permanent Flexible

Senior Specialist I, QA Clinical

The Senior Specialist I, QA Clinical is responsible for quality oversight in clinical development, supporting cross-functional relationships and ensuring compliance with GCP/GVP regulations. Key responsibilities include developing and implementing risk-based audit plans, conducting audits, and managing quality events. The role involves working closely with clinical project teams and external stakeholders, and maintaining the quality management system.

Autolus

Stevenage, United Kingdom