Latest Life Sciences Jobs

GSK logo

Director, Oncology Clinical Biomarkers

This role involves developing and implementing biomarker strategies to support the clinical development of late-stage oncology assets. Responsibilities include collaborating with cross-functional teams, validating biomarker strategies, and integrating them into clinical plans to optimize decision-making and patient stratification.

GSK United States £189,750 – £316,250 pa
On-site Permanent
GSK logo

Director, Oncology Clinical Biomarkers

This role involves developing and implementing biomarker strategies to support the clinical development of late-stage oncology assets. Responsibilities include collaborating with cross-functional teams, validating biomarker strategies, and integrating them into clinical plans to optimize decision-making and patient stratification.

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

Head, PV and Regulatory QA

TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...

CSL
CSL logo

Specialist, R&D Contracts & Business Operations

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an...

CSL
AstraZeneca logo

Feasibility and Recruitment Lead

This role involves leading UK feasibility and recruitment for cutting-edge cell therapy studies, translating scientific insights into actionable plans. Responsibilities include guiding end-to-end feasibility, collaborating with global stakeholders, and developing recruitment strategies to ensure timely and effective patient access to trials.

AstraZeneca Cambridge, United Kingdom
On-site Permanent

Clinical Scientific Expert (CSE) I

Salary Range:£37,593.50 - £69,816.50Job Description SummaryWork Arrangement: Hybrid Working, #LI-HybridLocation: London (The Westworks), United KingdomRelocation Support: This role is based in London, United Kingdom. Novartis is unable to offer relocation support: please only apply if accessible.ABOUT THE ROLEThe Clinical Scientific...

Novartis London, United Kingdom

Trial Vendor Senior Manager - Global Clinical Operations

This role involves end-to-end management of clinical trial vendors, ensuring timely and compliant delivery of services such as eCOA, central labs, and IRT. The Senior Manager leads vendor performance, financial oversight, and system validation activities while collaborating across global teams to support trial execution. Focus areas include risk mitigation, site activation, and adherence to GxP and ICH standards within a hybrid working model.

Novartis London, United Kingdom £49,140 – £91,260 pa
Hybrid Permanent
Pfizer logo

VMG Access Technology & Operations Lead

This role involves leading the advancement of AI, digital tools, and operational capabilities across VMG Access at Pfizer. Responsibilities include driving technology strategy, implementing AI and automation, shaping GTCS-related changes, enabling data-driven decision-making, and ensuring compliance and risk management.

Pfizer Spain
On-site Permanent Flexible
Pfizer logo

VMG Access Technology & Operations Lead

This role involves leading the advancement of AI, digital tools, and operational capabilities across VMG Access at Pfizer. Key responsibilities include driving technology strategy, leading AI and automation initiatives, shaping GTCS-related technology changes, and enabling data-driven decision-making to support strategic and operational insights.

Pfizer London, SW7 2AP, United Kingdom
Hybrid Permanent

Regulatory Operations Specialist

This role involves supporting regulatory compliance and submissions for product development within a regulated life sciences environment. The specialist will advise on global regulatory standards, coordinate submissions, review documentation and labelling, and work closely with cross-functional teams to ensure alignment with commercial and compliance objectives. It is a contract position with hybrid working in Bracknell.

Carbon 60 Bracknell, Berkshire, United Kingdom £23 ph
Hybrid Contract

Regulatory Affairs Specialist

The role involves providing technical regulatory support for the international distribution of diagnostic products, ensuring compliance with CE marking and global medical device regulations. Responsibilities include validating product claims, maintaining up-to-date documentation, and reviewing complaints for regulatory reportability. The position is based at the Innovation Centre in Bedford with hybrid working options.

Swiss Precision Diagnostics GmbH Cardington, Bedfordshire, United Kingdom £30,000 – £35,000 pa
Hybrid Contract
Roche logo

Safety Process Director / Senior Safety Process Director

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

Head of Engineering & Product Development

Head of Engineering & Product DevelopmentLocation: Lancing, Sussex (onsite)Salary: Competitive + BenefitsAn exciting opportunity has arisen for an experienced engineering leader to take ownership of an R&D team within a growing organisation operating in the medical devices / highly regulated...

CBSbutler Holdings Limited trading as CBSbutler Lancing, West Sussex, United Kingdom
Roche logo

Field Service Representative (Hampshire/Dorset area)

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 United Kingdom

Project Quality Lead

This role involves leading quality strategy across the full product lifecycle in a pharmaceutical development environment. You'll drive design reviews, risk management, and quality system implementation while working closely with project teams and stakeholders. The position emphasizes proactive quality integration rather than post-hoc review, with a focus on influencing technical decisions and ensuring compliance through GMP and ISO standards.

Next Phase Recruitment United Kingdom
On-site Contract