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Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development will lead clinical research activities for GSK’s oncology portfolio, collaborating with various stakeholders to develop and execute phase 1-3 clinical trials. Key responsibilities include protocol development, medical monitoring, safety data review, and strategic partnerships with key external experts.

GSK

Stevenage, United Kingdom

Hybrid Permanent

Vaccines Safety Sciences Lead

Leads and manages pharmacovigilance and safety sciences functions, ensuring compliance with global regulatory standards and GxP guidelines. Oversees signal detection, safety data analysis, and regulatory documentation such as the PSMF, while driving process improvements and supporting PV inspections. Acts as a strategic expert in implementing safety systems and translating business requirements into technical solutions for global teams.

CSL

On-site Permanent

Technical Program Coordinator, DDMR, London

As a Technical Program Coordinator, you will support the Drug Design and Medical Research (DDMR) function by managing program planning, monitoring timelines, tracking actions, and reporting risks. You will work closely with drug design teams, internal stakeholders, and external partners to ensure effective communication and alignment across the organization.

Isomorphic Labs

London, United Kingdom

£26 ph On-site Permanent Clearance Required

Band 6 Specialist Biomedical Scientist Haematology

As a Specialist Biomedical Scientist in Haematology and Blood Transfusion, you will work across central and satellite laboratories, processing and analysing patient samples, performing complex tests, and maintaining high standards of quality and safety. You will also support junior staff, manage stock, and participate in out-of-hours duties.

NHS Professionals

Walton, Buckinghamshire, Buckinghamshire, HP21 7RY, United Kingdom

Hybrid Permanent

Associate Director Audit & Assurance R&D Q&A

Leads risk-based GxP audit programs in R&D, focusing on GVP and GCP compliance to support clinical trials and regulatory readiness. Drives inspection preparedness, supplier qualification, and CAPA management while advising on quality systems across innovative areas like AI, cell therapy, and digital health. Works cross-functionally to embed quality assurance into emerging scientific and technological platforms.

AstraZeneca

Chatham, ME4 4NP, United Kingdom

Sr. Manager, Site Budgets and Contracts

The RoleReporting to the Director, Global Clinical Operations (GCO) Business Analytics & Operations Management (BAOM), the Senior (Sr.) Manager, Site Budgets & Contracts will focus on the generation and review of investigator site budgets related...

Moderna

Oxford, United Kingdom