Latest Project Services Jobs

Director, Respiratory Innovation, Global Epidemiology and RWE

Leads global respiratory epidemiology and real-world evidence initiatives to shape vaccine development, designing and delivering studies on disease burden, treatment patterns, and safety. Works cross-functionally with clinical, regulatory, and external partners, driving scientific strategy and innovation. Involves mentoring staff, managing collaborations, and disseminating findings through publications and regulatory submissions.

GSK €123,000 – €205,000 pa

Associate Medical Director, Safety Evaluation and Risk Management (SERM)

This role involves providing medical and scientific leadership in safety evaluation and risk management for GSK’s clinical and post-marketing assets. The Associate Medical Director will lead safety strategy, contribute to regulatory submissions, and guide cross-functional teams in pharmacovigilance activities. The position emphasizes evidence-based decision-making, global regulatory compliance, and proactive risk communication within a matrix environment.

GSK United States €87,000 – €145,000 pa

Global Development Lead, Internal Medicine, Sr. Director (MD)

Leads clinical development for assigned assets in Internal Medicine, driving global clinical strategy, trial design, execution, and regulatory submissions. Serves as primary clinical accountability, collaborating with cross-functional teams and external stakeholders to advance drug development programs from concept through approval, with potential focus on obesity-related therapeutics.

Pfizer £274,500 – £457,500 pa

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

This role leads clinical development for Internal Medicine assets within Pfizer's Research & Development division, with accountability for designing and executing global clinical development plans. The position involves leading cross-functional teams, driving regulatory submissions, and serving as a therapeutic expert in obesity and related areas. It requires collaboration with internal and external stakeholders, including regulatory authorities and advisory boards, to shape clinical strategy and ensure successful drug development.

Pfizer

On-site Permanent

Research Scientist (Applied LLMs), London

A Research Scientist focused on applying Large Language Models to drug discovery, working in interdisciplinary teams to develop novel AI-driven approaches for biological and chemical challenges. The role involves advancing LLM techniques such as post-training, reasoning, tool-use, and alignment within a cutting-edge AI research environment. Collaboration with scientists and engineers is central to developing predictive models that accelerate rational drug design.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Research Scientist (Machine Learning), London

A Research Scientist in Machine Learning will develop novel deep learning models and algorithms to advance drug discovery at digital speed. Working in an interdisciplinary environment, they will apply cutting-edge ML techniques to complex biological and chemical problems, iterating closely with domain experts. The role involves leading high-ambition research projects, scaling training frameworks, and shaping the technical direction of AI-driven drug design.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

(Fixed Term) Laboratory Technician, Clinical Biomarker Laboratory, Immunoassay

This role involves hands-on laboratory work supporting immunoassay development and clinical testing for Moderna’s mRNA-based therapeutic programs. The technician will prepare reagents, conduct sample analysis, ensure regulatory compliance, and contribute to high-quality data generation for clinical trials. Based in Oxford, the position requires full-time on-site work in a regulated lab environment with occasional overtime.

Moderna Oxford, United Kingdom

On-site Contract

Associate Director, CMC Regulatory Affairs, International

This role involves leading CMC regulatory strategies for international submissions, including IND/CTA/BLA/MAA filings, with a focus on mRNA-based medicines. The individual will guide global regulatory compliance, interact with health authorities, and support quality and manufacturing teams across therapeutic areas like vaccines, oncology, and rare diseases. It requires deep expertise in biologics CMC regulations and a proactive approach to navigating complex regulatory landscapes.

Moderna London, United Kingdom

On-site Permanent

Senior Mechanical Engineer

Design and develop advanced electro-mechanical systems for medical technology applications, from concept through to manufacture. Work within a multidisciplinary team to solve complex engineering challenges and ensure compliance with regulatory standards. Contribute to innovative products that have a real-world impact on healthcare.

AES Ely, Cambridgeshire, United Kingdom £50,000 – £75,000 pa

Hybrid 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

Senior Modelling Scientist - San Sebastián - Fully

Lead complex mathematical and simulation-based modelling projects in bioprocessing and life sciences within a high-growth, well-funded start-up. Work autonomously on advanced technical challenges with opportunities for long-term career development in a remote-first environment. Collaborate with a growing team focused on accelerating technology through advanced modelling.

Newton Colmore Spain, United Kingdom

Remote

Senior Systems Engineer

This role involves leading the design, testing, and verification of electromechanical systems in medical devices, with a focus on improving reliability and supporting technology transfer to production. The engineer will conduct root cause analyses, optimize system performance, and lead cross-functional design reviews. Work spans system integration, validation, and documentation within a regulated healthcare technology environment.

GxPeople Global Trowbridge, Wiltshire, BA14 8EY, United Kingdom £65,000 – £75,000 pa

Firmware Engineer - TechBio

Design and develop C++ firmware for embedded systems and multiparametric probes, implementing control algorithms and working across the full firmware lifecycle from theory to production. Focus on debugging, validation, and optimisation within a TechBio innovation environment. Role involves close collaboration with sensor technology and machine learning integration.

Newton Colmore Guatemala

Senior / Principal Bioinformatician

Process and analyse multi-omic clinical datasets including RNAseq, NGS, and proteomics to derive biological insights supporting drug development decisions. Develop and optimise computational pipelines, integrate omics data with clinical variables, and contribute to scientific reporting and publications. Work autonomously within a collaborative, science-driven team across therapy areas such as oncology, neuro, and inflammation.

Hays Life Sciences London, United Kingdom

Member of Technical Staff

Design and develop novel generative machine learning models for protein design, integrating with wet lab experiments to validate performance in real-world biological contexts. Collaborate closely with interdisciplinary teams of researchers, engineers, and biologists while maintaining robust, scalable code and infrastructure. Focus on rapid prototyping, model optimization, and continuous learning from experimental feedback to advance synthetic biology.

Latent Labs London, United Kingdom, United Kingdom

Hybrid Permanent