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Hybrid Permanent

Director, Regional Ecosystem Lead (Northern Europe & UK)

This role involves leading CSL's presence in key innovation hubs across Northern Europe and the UK, building strategic relationships with biotech, academia, and investment networks. The Director will source and evaluate opportunities, lead deal teams, and represent CSL at industry events to enhance the company's reputation and deal flow.

CSL

United Kingdom

On-site Permanent

Associate Director, Safety Epidemiology – Global Patient Safety

Lead the design and execution of post-authorisation safety studies using real-world data to assess and communicate the safety profiles of AstraZeneca’s medicines. Provide strategic epidemiological input to regulatory submissions, safety signal evaluations, and diversity initiatives, collaborating with internal teams and external partners. Drive methodological excellence in pharmacoepidemiology and contribute to global patient safety decision-making across a broad product portfolio.

AstraZeneca

Chatham, ME4 4NP, United Kingdom

Hybrid Permanent

Associate Director, R&D Project Management

Leads the operational delivery of high-impact, global R&D projects within a cross-functional biotech environment. Focuses on strategic planning, budget and timeline management, risk mitigation, and stakeholder reporting. Provides mentorship to junior project management staff and ensures robust project execution across drug research, development, and manufacturing.

CSL

On-site Temporary

(Fixed Term) Manufacturing Associate I

Operate and maintain mRNA vaccine production equipment in compliance with cGMP and safety standards, executing manufacturing processes, troubleshooting equipment and digital systems, and supporting quality documentation and continuous improvement initiatives. Work within a cross-functional team to ensure timely batch release and operational excellence in a fast-paced, highly regulated environment.

Moderna

Oxford, United Kingdom

US$222,750 – US$371,250 pa Hybrid Permanent

Medical Director, Oncology Clinical Development

This role involves leading oncology clinical trials from protocol design to study reporting, ensuring scientific integrity and alignment with regulatory and commercial goals. The Medical Director will collaborate with global experts and internal teams to advance GSK’s oncology pipeline, with a focus on data generation, safety monitoring, and strategic medical input across the clinical development lifecycle.

GSK

Stevenage, 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