Latest IT Recruitment Jobs

Global Labelling Manager, Content (Neuroscience)

The Global Labelling Manager, Content will lead the development and maintenance of high-quality global labelling documents for pharmaceutical products. Key responsibilities include organising cross-functional discussions, conducting research on competitor labels, and ensuring compliance with regulatory standards across different markets.

Novartis

Hybrid Permanent

Global Labelling Associate Director, Content (Oncology)

This role involves developing and maintaining global labelling strategies and core documents for oncology products. You will lead cross-functional discussions, present proposals to governance bodies, and ensure compliance with regulatory requirements across global markets.

Novartis

Hybrid Permanent

Global Labelling Associate Director, Content (Established Products)

This role involves developing and maintaining global labelling strategies and core documents for pharmaceutical products. You will lead cross-functional discussions, present labelling proposals, and ensure compliance with regulatory requirements across different markets.

Novartis

Hybrid Permanent

Maintenance Engineer

Maintenance EngineerStarting Salary £33,419 - £37,582 per annum (plus opportunities for paid overtime)Open-ended and full-timeMRC Laboratory of Molecular Biology, Cambridge Biomedical Campus, UKThe MRC Laboratory of Molecular Biology, Cambridge (LMB) is an internationally recognised scientific research institution.We are looking to...

MRC Laboratory of Molecular Biology Great Shelford, Cambridgeshire, United Kingdom £33,419 – £37,582 pa

Senior Principal Developer

This role involves developing and maintaining R packages and Shiny applications to support clinical trial data analysis, automation, and reporting workflows. The developer will collaborate with statisticians and clinical teams to deliver efficient, reproducible tools, while promoting best practices in data science and software development. A strong focus is placed on responsible AI integration, open-source collaboration, and modernizing clinical reporting through user-centric design and tooling.

Novartis London, United Kingdom £57,050 – £105,950 pa

Hybrid Permanent

Director Data Science & Agentic AI

Leads the design and deployment of agentic AI systems—such as multi-agent architectures and tool-using LLMs—within Novartis' Global Drug Development to accelerate drug development timelines. Responsible for technical execution, governance, and strategic direction of AI initiatives across clinical, translational, and regulatory domains. The role involves building evaluation frameworks, ensuring regulatory compliance, mentoring AI teams, and driving innovation through research and external collaboration.

Novartis London, United Kingdom £100,240 – £186,160 pa

Hybrid Permanent

Biomedical Scientist

Biomedical Scientist | Pathology | Full Time | Perm | ManchesterWe're looking for a motivated Biomedical Scientist to join our Pathology team at Manchester Hospital. This full‑time, role offers the chance to work in a supportive, well‑equipped laboratory while playing...

Spire Healthcare Manchester, United Kingdom

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

This role involves developing and maintaining global labelling strategies and documents for cardiovascular, renal, and metabolic products. You will lead cross-functional discussions, present labelling proposals, and ensure compliance with regulatory requirements across global markets.

Novartis London, United Kingdom

Hybrid Permanent

Medical Laboratory Assistant

Process and handle patient specimens in a hospital laboratory, ensuring accurate data entry and adherence to quality and safety standards. Perform basic testing, maintain equipment, and support diagnostic workflows within a fast-paced healthcare environment. Work as part of a team to sustain efficient laboratory operations and contribute to patient care.

Acorn by Synergie Lansdown, Somerset, United Kingdom £13 – £15 ph

On-site Temporary

Senior Medical Writer, Pharmacovigilance

Your new companyAre you an experienced Senior Medical Writer looking for your next long-term contract opportunity?I am currently partnering with a leading global pharmaceutical organisation seeking a Senior Medical Writer to join their clinical and regulatory writing team on an...

Hays Life Sciences High Welwyn, Hertfordshire, United Kingdom £46 – £75 ph

Clinical Development Director - Renal

The Clinical Development Director is responsible for leading and supporting the delivery of clinical deliverables for a section of a global clinical program or a large, complex trial. This role involves collaborating with various teams to ensure data quality, regulatory compliance, and scientific accuracy in clinical trials and publications.

Novartis London, United Kingdom

Hybrid Permanent

Precision Medicine Director

The Precision Medicine Director leads biomarker and diagnostic strategy development for global clinical programs in neuroscience, ensuring alignment with regulatory and clinical objectives. This role involves leading cross-functional teams, designing patient selection approaches, and supporting regulatory submissions. The position operates at the intersection of clinical development, diagnostics, and precision medicine, with a strong focus on scientific rigor and compliance.

Novartis London, United Kingdom

Hybrid Permanent

Precision Medicine Director

Job Description Summary#LI-HybridWork Arrangement: Hybrid WorkingNovartis is unable to offer relocation support: please only apply if accessible.The Precision Medicine Director is responsible for developing and executing precision medicine strategies aligned to disease area and clinical program objectives. This role leads...

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom

Global Program Clinical Head (Neuroscience)

As a Global Program Clinical Head, you will lead end-to-end clinical development programs in Neuroscience, driving strategy, execution, and regulatory compliance. You will collaborate with global teams, influence key decisions, and ensure patient-centric clinical trials.

Novartis London, United Kingdom

Risk Surveillance Lead

The Risk Surveillance Lead drives the adoption of RBQM practices in clinical trials, overseeing risk assessment, documentation, and continuous improvement. They work closely with cross-functional teams to ensure quality risk management and compliance with regulatory standards.

Novartis London, United Kingdom

Hybrid Permanent