Latest Project Services Jobs

Senior Scientific Writer II

The Senior Scientific Writer II role involves developing high-quality medical and scientific communications for Novartis, including slide decks, congress materials, and advisory board content. The position requires strong collaboration with cross-functional teams to ensure content accuracy, consistency, and compliance with internal and external standards.

Novartis London, United Kingdom

Hybrid Permanent

Embedded Software Lead

Embedded Software Lead - Medical DevicesBristol + Hybrid Work from HomeUp to £80,000 + Bonus, OTE £100,000KO2's client is an innovative and fast-growing medical technology business developing advanced devices in a regulated environment. They are looking for an Embedded Software...

KO2 Embedded Recruitment Solutions Bristol, Bristol (county), United Kingdom £70,000 – £80,000 pa

Senior Principal Developer

This role involves developing and maintaining R packages and Shiny applications to support clinical trial data analysis and reporting. The developer will collaborate with statisticians and clinical teams to build automated, reproducible tools, while promoting open-source practices and responsible AI integration. Emphasis is placed on modernizing workflows through user-centric design, documentation, and deployment in production environments.

Novartis £57,050 – £105,950 pa

Remote Permanent

Computational Protein Designer

Computational Protein DesignerThe opportunityWe are seeking a Computational Protein Design Scientist to join our team working at the interface of generative AI and synthetic biology. Working closely with our Lead Computational Protein Designer, you will play a key role amongst...

Latent Labs London, United Kingdom, United Kingdom

Hybrid Permanent

Member of Technical Staff, Applied AI

Member of Technical Staff, Applied AIThe opportunityWe are looking for a Member of Technical Staff with deep expertise in generative modelling to work at the interface between our frontier models and the customers who depend on them. You will join...

Latent Labs London, United Kingdom, United Kingdom

Hybrid Permanent

Forward Deployed AI Engineer

Forward Deployed AI EngineerThe opportunityWe are looking for a Forward Deployed AI Engineer to serve as the critical bridge between Latent Labs’ frontier generative models and the customers who rely on them. You will work directly with pharmaceutical and biotech...

Latent Labs London, United Kingdom, United Kingdom

Hybrid Permanent

Quality Systems Officer (QMS)

The Quality Systems Officer will support the maintenance of the Quality Management System (QMS), manage quality documentation, and assist with CAPAs, deviations, and change controls. This role involves working closely with the Quality team to ensure compliance with GMP standards and participate in continuous improvement initiatives.

Russell Taylor Group Sk91Al, SK9 1AL, United Kingdom £30,990 pa

On-site Permanent

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data and documentation to ensure accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve data discrepancies and maintain inspection readiness.

Moderna Oxford, United Kingdom

On-site Temporary

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data and documentation to ensure accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve discrepancies and maintain inspection readiness.

Moderna

On-site Temporary

Regulatory Science Professional - Intelligence

This role involves managing regulatory intelligence for Roche’s pharmaceutical and medical device portfolio in the EU, with a focus on generating strategic, data-driven insights. The professional will leverage AI tools, maintain regulatory databases, and collaborate across global teams to inform decision-making and drive innovation in a dynamic regulatory environment.

Roche Welwyn Hatfield, United Kingdom

Hybrid Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for global R&D trials, translating protocols into operational supply strategies, and ensuring on-time delivery of investigational products. The Clinical Trial Supply Manager acts as the key link between clinical teams and supply operations, overseeing demand planning, depot management, and compliance across Phase I–IV studies, including investigator-sponsored and compassionate use trials.

GSK Stevenage, United Kingdom €48,375 – €116,000 pa

On-site Permanent

Senior Director, Head of AI for Clinical Development, Early BPRD

This role involves leading the development and application of AI in early phase clinical trials for AstraZeneca, focusing on Phase I/II programs. You will build and manage a team of AI researchers and engineers, develop reusable AI methods, and collaborate with domain experts to improve clinical trial design and decision-making.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

(Fixed Term) Analyst, Quality Control, Microbiology

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization,...

Moderna Oxford, United Kingdom

(Fixed Term) Analyst, Quality Control, Microbiology

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization,...

Moderna Gargrave, BD23 3RZ, United Kingdom

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for GSK’s global R&D studies, translating protocols into operational supply strategies, and ensuring timely delivery of investigational products. The manager will coordinate across depots, logistics partners, and clinical teams to maintain supply continuity, minimise waste, and support study milestones across phases I–IV. It requires strong planning, risk management, and GxP compliance in a patient-focused, global trial environment.

GSK Belgium €69,600 – €116,000 pa

On-site Permanent