Latest Drug Discovery Jobs

ML Research Engineer, London

Develop and optimise cutting-edge AI models at the intersection of machine learning and drug discovery, translating research into scalable, production-ready systems. Work on foundational models like Diffusion networks, Transformers, and GNNs, building robust infrastructure and data pipelines while collaborating closely with scientists. Focus on advancing a digital biology platform to accelerate rational drug design across multiple therapeutic areas.

Isomorphic Labs London, United Kingdom

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

Medical Director, Oncology Clinical Development - GU

This role involves providing medical leadership within GSK's oncology clinical development team, focusing on genitourinary (GU) cancers. The Medical Director will lead medical monitoring, ensure patient safety, interpret clinical data, and contribute to study design and regulatory submissions. Working closely with cross-functional teams, the role integrates physician-level insight into clinical strategy and drug development execution.

GSK Stevenage, United Kingdom £472,500 – £787,500 pa

Medical Director-Oncology Clinical Development - GI

This role involves leading medical oversight in gastrointestinal (GI) oncology clinical development, ensuring patient safety and clinical integrity across study design, execution, and data interpretation. The Medical Director collaborates with cross-functional teams to integrate physician insights into clinical trials, engages with external experts and regulators, and contributes to regulatory submissions and scientific communications. The position requires deep expertise in oncology and clinical development within a global pharmaceutical environment.

GSK United Kingdom £222,750 – £371,250 pa

Analyst, Quality Control, Microbiology

This role involves performing routine environmental monitoring, water sampling, and microbiological testing to support GMP quality control for mRNA products. The analyst will execute tests including sterility, bioburden, endotoxin, and TOC, while supporting method transfers, validations, and compliance with cGMP standards. The position requires strong documentation practices, collaboration with cross-functional teams, and active participation in quality systems such as investigations and audits.

Moderna

On-site Permanent

Analyst, Quality Control, Microbiology

This role involves performing routine environmental monitoring, water sampling, and microbiological testing (including sterility, bioburden, and endotoxin) for mRNA products in a GMP-regulated manufacturing environment. The analyst will support method transfers, data review, investigations, and compliance activities while working closely with internal teams and contract laboratories. Emphasis is placed on digital workflows, data integrity, and adherence to cGMP standards.

Moderna Oxford, United Kingdom

Central Monitor (Data Surveillance Lead)

The Central Monitor (CM) oversees and supports clinical trials through centralized monitoring activities, ensuring data quality, identifying risks, and enhancing trial oversight. They collaborate with cross-functional teams, configure Central Monitoring technology, and provide ongoing data surveillance and risk management.

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

Innovation Capability Director - Global Clinical Operations (GCO)

This role involves leading the identification, implementation, and scaling of innovative patient recruitment solutions for clinical trials. The director will work with global teams and technology partners to transform ideas into scalable capabilities, focusing on digital marketing and AI-driven approaches to improve patient engagement and trial participation.

Novartis £83,510 – £155,090 pa

Maintenance Engineering Manager - Packaging

Lead the technical development and implementation of a new labeling and secondary packaging operation at Moderna’s Harwell site, from initial design through commissioning and validation. Establish maintenance strategies, ensure GMP compliance, and drive continuous improvement using engineering excellence principles and digital tools. Build and lead a high-performing engineering team to support long-term operational success in a regulated biotech environment.

Moderna

Hybrid Permanent

Associate Director, CMC Regulatory Science, International

This role involves leading CMC regulatory strategy for global mRNA product development, preparing and reviewing regulatory submissions, and guiding cross-functional teams on compliance and agency interactions. The position requires deep expertise in biologics CMC regulations, particularly in EU and ROW markets, and plays a key part in shaping regulatory pathways across vaccines, oncology, and rare diseases. Based at the Harwell site, it emphasizes in-office collaboration within a multidisciplinary team.

Moderna

On-site Permanent

Scientist, Genetic Assays

This role involves developing and executing biochemical and molecular biology assays to support pharmacokinetic/pharmacodynamic analysis. Responsibilities include assay development, data analysis, and collaboration with external partners, while staying current with scientific literature and regulatory guidelines.

Moderna

(Fixed-Term) Manufacturing Associate I

Operate and maintain equipment in a cGMP-compliant, highly automated mRNA vaccine production environment at Moderna's Oxford facility. Perform production operations, support quality assurance, troubleshoot issues, and contribute to continuous improvement initiatives using digital systems and advanced manufacturing technologies. Work within a 2-2-3 rotating shift pattern to ensure reliable, safe, and compliant vaccine manufacturing.

Moderna Oxford, United Kingdom

Sr. Manager, Site Budgets and Contracts

This role involves leading the creation and management of investigator site budgets and contracts for clinical trials, using Grants Manager and FMV benchmarking tools. The candidate will oversee CRO activities, ensure budget consistency across trials, and support timely site activation by managing negotiations and identifying risks. Collaboration with legal, clinical operations, and external partners is central to ensuring compliance and efficiency in contract execution.

Moderna Oxford, United Kingdom

(Fixed-Term) Manufacturing Associate I

This role involves operating and maintaining equipment in a cGMP-regulated mRNA vaccine production environment, ensuring safe and compliant manufacturing processes. The associate will execute production operations, support quality assurance, troubleshoot technical issues, and contribute to continuous improvement initiatives. Work is conducted in a highly automated, digitally enabled facility with a focus on operational excellence and innovation in mRNA technology.

Moderna

Senior Manager, Government Affairs – UK

This role involves shaping and executing Moderna’s Government Affairs strategy across the UK, with a focus on enabling innovative mRNA-based respiratory vaccines through policy engagement. The individual will build relationships with government, Parliament, and healthcare stakeholders, translate political and policy trends into strategic positions, and leverage AI tools to enhance policy intelligence. Collaboration across internal teams and external partners is key to influencing public policy and supporting Moderna’s mission in a fast-paced, innovation-driven environment.

Moderna London, United Kingdom