Biotechnology Jobs

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

On-site Permanent

Biologics Account Manager

This role involves driving adoption of respiratory biologics within secondary care settings by building strategic relationships with multi-disciplinary teams and key healthcare stakeholders. The Account Manager will lead formulary access, support homecare utilization, and execute account plans in a complex clinical environment. It requires strong commercial acumen, deep understanding of the NHS ecosystem, and the ability to navigate multi-stakeholder decision-making units.

AstraZeneca Sheffield, United Kingdom

On-site Permanent

Associate Engineer, GxP IT Support

This role involves supporting Moderna’s manufacturing operations at the Harwell site, ensuring GMP compliance and providing Tier 1 IT support. Responsibilities include maintaining robust IT systems, triaging incidents, managing infrastructure, and collaborating with various teams to ensure smooth operations. The position offers exposure to modern cybersecurity and automation tools, making it a dynamic and challenging opportunity in the biotech industry.

Moderna

On-site 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 US$222,750 – US$371,250 pa

Hybrid Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK’s global assets, with a focus on immunology. The Scientific Director will evaluate safety data, lead cross-functional teams, and ensure compliance in clinical development and post-marketing settings. The position requires deep expertise in safety evaluation, signal detection, and international regulatory standards.

GSK US$169,950 – US$283,250 pa

On-site 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

Hybrid Permanent

Vaccines Safety Sciences Lead

Leads and manages pharmacovigilance functions, ensuring compliance with global regulatory standards and GxP guidelines. Oversees signal detection, safety data analysis, and regulatory documentation while providing strategic direction for process improvements and inspection readiness. Acts as a subject matter expert in safety sciences, leading teams and contributing to drug development and post-marketing safety initiatives.

CSL

Hybrid 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

On-site Permanent

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 £26 ph

On-site Permanent Clearance Required

Head of Medicinal Chemistry, Drug Design, London

As Head of Medicinal Chemistry, you will lead a team of 25 chemists in London, driving the development of novel drugs using cutting-edge AI and machine learning. You will provide strategic direction, mentor team members, and collaborate with AI/ML scientists to accelerate drug discovery and clinical candidate nomination.

Isomorphic Labs London, United Kingdom

On-site Permanent

Master Scheduler, Engineering

Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...

Autolus Stevenage, United Kingdom

Senior Executive Assistant to CEO

This role involves providing high-level executive support to the CEO of a clinical-stage TechBio company, managing a complex calendar, travel, and communications while serving as a key liaison across global teams and stakeholders. The position requires exceptional organizational skills, discretion, and proactive problem-solving to enable the CEO’s strategic focus. Based in New York, the role supports a fast-paced, innovation-driven environment spanning biotechnology and AI.

Recursion North Tyneside, NE29 8EP, United Kingdom US$130,460 – US$164,780 pa

On-site Permanent

Global Clinical Study Lead

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive...

Roche Welwyn Hatfield, United Kingdom

Director, CMC Regulatory Affairs

Lead the development and execution of global CMC regulatory strategies for small molecule drugs in clinical trials and marketing applications. Author and manage high-quality regulatory submissions across the US, EU, and rest of world, while advising cross-functional teams on compliance, risk mitigation, and evolving GMP standards. Collaborate closely with internal and external stakeholders to ensure timely delivery of regulatory deliverables and support clinical development programs.

Recursion London, W1C 2QP, United Kingdom

Remote Permanent