Latest Life Sciences Jobs

Head of RTSM (Randomization and Trial Supply Management)

Lead the design and delivery of Randomization and Trial Supply Management (RTSM) strategies across global clinical trials, ensuring reliable supply and randomization systems for patient-focused studies. Partner with cross-functional teams and external vendors to optimize processes, ensure compliance, and support clinical trial execution from Phase I–IV. This role emphasizes leadership in process improvement, team development, and integration of RTSM within broader clinical operations.

GSK United States

Hybrid Permanent

SERM Scientific Director

Leads safety evaluation and risk management for GSK's oncology assets in clinical development, providing scientific expertise to assess and communicate safety risks globally. Works cross-functionally to shape safety strategy, support regulatory submissions, and ensure patient protection. Focuses on signal detection, risk assessment, and strategic decision-making in a matrix environment.

GSK £111,750 – £186,250 pa

On-site Permanent

Global Labelling Director (Team Lead), Content

Leads a team of labelling professionals to develop and maintain global labelling strategies and content for pharmaceutical products. Ensures compliance with regulatory requirements and alignment with product development and lifecycle plans through close collaboration with cross-functional teams and regulatory authorities. Focuses on continuous improvement of labelling processes and high-quality, science-driven documentation.

Novartis London, United Kingdom

Hybrid Permanent

Application Engineer

The role involves supporting technical sales and customer relationships for microfluidic systems, handling pre- and post-sales activities including quoting, CRM management, and customer support. The engineer will collaborate with technical teams to meet client requirements and represent the company at trade events. It offers exposure to international projects across diverse sectors such as life sciences and space.

Jackson Hogg Gateshead, Tyne & Wear, United Kingdom £30,000 – £32,000 pa

Clinical Development Director - Renal

The Clinical Development Director leads and supports clinical development activities within a global program, focusing on strategy, trial execution, data analysis, and regulatory documentation. This role involves close collaboration with cross-functional teams, ensuring scientific rigor and data quality across phases I–IV trials, particularly in late-phase development. The position requires strong scientific expertise, leadership in clinical operations, and active participation in safety and regulatory initiatives.

Novartis London, United Kingdom

Hybrid Permanent

Immunohistochemistry Scientist

Perform hands-on development and optimisation of automated immunohistochemistry (IHC) assays in a preclinical research environment. Independently design experiments, analyse data, and contribute to client projects requiring scientific rigour and regulatory compliance. Support study reporting, troubleshooting, and process improvement within a GLP/GxP-aligned laboratory setting.

RBW Consulting Royston, Hertfordshire, United Kingdom

On-site Permanent

Field Service Representative (Hampshire/Dorset area)

This role involves providing frontline technical support for Roche’s diagnostic equipment within NHS pathology laboratories across the Hampshire/Dorset region. The Field Service Representative will perform proactive and reactive maintenance on electro-mechanical systems, troubleshoot technical faults, and minimise equipment downtime using digital tools. Additional responsibilities include delivering training to laboratory staff and participating in customer review meetings, ensuring high standards of service delivery.

Roche United Kingdom

Regional Operations Manager - Engineering

Oversee regional operations for engineering projects, ensuring on-time, on-budget delivery while managing multidisciplinary teams and cross-functional collaboration. Drive operational excellence through KPI monitoring, risk mitigation, and continuous improvement initiatives. Support commercial growth by aligning technical capabilities with strategic customer needs and contributing to innovation across global teams.

Averna Powered By Spherea East Parley, Dorset, United Kingdom

Radiopharmaceutical QP

CMDO is Seeking to Appoint a Qualified Person. The Organisation is Engaged in Developing and Manufacturing New Medicines and Novel Formulations, Including a Wide Range of Oral Solid and Liquid Dosage Forms, Sterilised and Aseptically Filled Products, as well as...

CV-Library City of Westminster, Greater London

Senior Manager, Trade Operations & Compliance, EMEA

Lead and shape trade compliance strategy across EMEA, ensuring seamless cross-border movement of medicines through robust customs and regulatory frameworks. Drive digital transformation in trade operations using tools like SAP GTS and AI-enabled solutions, while collaborating with cross-functional teams to optimize compliance, reduce costs, and enhance operational agility. Serve as a key liaison with customs authorities and internal stakeholders to maintain regulatory readiness and operational excellence.

Moderna Breckland, IP24 1HF, United Kingdom

Research Fellow (Bioinformatics)

Develop and deploy scalable bioinformatics pipelines and cloud-based infrastructure to support genomics and multi-omics research within a collaborative, industry-led translational research environment. Work closely with biologists and software developers to integrate advanced computational methods with cloud platforms like AWS, Azure, or GCP. Focus on streamlining data analysis workflows and enhancing data sharing across interdisciplinary projects.

Queen's University Belfast Belfast, United Kingdom £41 pa

Contract

Vaccines Safety Sciences Lead

Leads and manages pharmacovigilance safety sciences functions, ensuring compliance with global regulatory standards and overseeing signal detection, safety data analysis, and process optimization. Provides strategic direction for evolving PV legislation and acts as a subject matter expert in audits and inspections. Supports drug development and post-marketing safety reporting while driving data visualization and analytical improvements.

CSL

Hybrid Permanent

Vaccines Safety Sciences Lead

Leads vaccine safety sciences functions, ensuring compliance with pharmacovigilance regulations and global safety standards. Oversees signal detection, safety data analysis, and regulatory documentation while guiding process improvements and cross-functional initiatives. Manages teams and supports regulatory inspections, safety reporting, and the implementation of data visualization tools for enhanced decision-making.

CSL

Hybrid Permanent

Senior Scientist (In vivo Pharmacology & Translational Sciences), Cambridge, MA

Lead translational strategies for oncology and immunology programs by designing in vivo pharmacology and PK/PD studies to validate AI-designed drug candidates. Bridge computational predictions with experimental validation through CRO partnerships and biomarker-driven approaches. Drive preclinical data generation to inform clinical trial design and regulatory filings.

Isomorphic Labs England

Hybrid Permanent

Senior Director Project Toxicologist

This role involves leading regulatory toxicology strategies for late-stage clinical and marketed products across multiple therapy areas, with a focus on safety risk assessment and global marketing applications. The Senior Project Toxicologist provides non-clinical safety expertise, supports regulatory submissions, and mentors teams through the drug development lifecycle. Based in Cambridge, the position operates within a collaborative R&D environment, requiring deep scientific and regulatory knowledge in toxicology.

AstraZeneca Cambridge, United Kingdom