Latest Drug Discovery Jobs

Bioanalytical Lead, London

Lead the development and execution of bioanalytical strategies for a diverse portfolio of AI-designed therapeutics, including small molecules, biologics, and ADCs. Design and validate PK, PD, and immunogenicity assays, manage global CROs, and integrate bioanalytical data into AI models to refine drug discovery. Play a key role in IND-enabling studies and cross-functional preclinical development in a hybrid London-based role.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Associate Director, Clinical Supply Chain, Cambridge, MA

This role involves leading end-to-end clinical trial material planning, vendor management, packaging, labeling, inventory management, and global distribution. You will work closely with Clinical Operations and the Clinical Development team to ensure seamless clinical trial execution and compliance with regulatory standards.

Isomorphic Labs Cambridge, United Kingdom

Medical Director-Oncology Clinical Development - GI

This role involves leading medical monitoring and safety oversight for gastrointestinal (GI) oncology clinical trials within GSK’s global development programme. The Medical Director provides physician-level expertise in study design, data interpretation, and regulatory engagement, ensuring patient safety and clinical integrity across phases I–III. Working within a cross-functional matrix team, the role integrates medical insight into clinical strategy and collaborates with external experts and investigators to advance innovative cancer therapies.

GSK

Hybrid Permanent

Medical Director, Oncology Clinical Development - GU

This role involves providing medical leadership within oncology clinical development, specifically in genitourinary (GU) cancers. The Medical Director will lead medical monitoring, ensure patient safety, contribute to study design and regulatory interactions, and interpret clinical data to inform decision-making. They will work closely with cross-functional teams and external experts to advance GSK’s oncology pipeline with a focus on high unmet need areas.

GSK Switzerland

Hybrid Permanent

Clinical Research Associate (Multiple Roles)

This role involves managing clinical trial sites across Phase I–IV studies, ensuring protocol compliance, data integrity, and patient safety. The Clinical Research Associate conducts site visits, delivers training, monitors performance, and drives risk mitigation in collaboration with cross-functional teams. It is a field-based, site-facing position requiring strong regulatory knowledge and relationship-building skills.

Novartis United Kingdom £32,690 – £60,710 pa

(Fixed-Term) Manufacturing Associate

This role involves hands-on mRNA vaccine production operations at Moderna’s Harwell facility, adhering to cGMP standards and collaborating with Quality Assurance. Responsibilities include operating production equipment, maintaining compliance, troubleshooting, and contributing to continuous improvement and digital innovation.

Moderna Oxford, United Kingdom

Global Regulatory Associate Director, Life Cycle Management

Manages regulatory maintenance for a high-complexity pharmaceutical portfolio, ensuring compliance and timely submissions. Develops strategic regulatory input for safety reports, variations, and renewals, while acting as a liaison with health authorities. Supports global approval processes and contributes to process improvements and team mentorship.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Warehouse Specialist, Logistics

This role involves hands-on warehouse operations at Moderna's Harwell facility, ensuring the seamless flow of materials for mRNA manufacturing. Responsibilities include managing inbound deliveries, maintaining inventory accuracy, and supporting manufacturing operations in a highly regulated GMP/GDP environment.

Moderna Oxford, United Kingdom

Maintenance Engineering Manager - Packaging

Lead the technical development and implementation of a new labeling and secondary packaging operation at Moderna's Harwell site, ensuring compliance with GxP and safety standards. Establish maintenance strategies, lead capital projects, and drive continuous improvement using engineering excellence principles. Work closely with global teams and support digital integration in a high-growth biotech environment.

Moderna Oxford, United Kingdom

Hybrid Permanent

Associate Director, CMC Regulatory Science, International

Lead the development and execution of CMC regulatory strategies for mRNA-based products across global submissions, including IND/CTA/BLA/MAA filings. Provide expert guidance on regulatory compliance, interact with health authorities, and support quality and manufacturing teams through change controls and submissions. Work within a multidisciplinary team at the Harwell site to advance Moderna’s pipeline in vaccines, oncology, and rare diseases.

Moderna London, United Kingdom

On-site Permanent

(Fixed-Term) Manufacturing Associate

This role involves hands-on mRNA vaccine production operations at Moderna’s Harwell facility, adhering to cGMP standards and collaborating with Quality Assurance. Responsibilities include operating production equipment, maintaining documentation, troubleshooting issues, and contributing to continuous improvement and digital innovation.

Moderna

Scientist, Genetic Assays

This role involves designing and executing biochemical and molecular biology assays to support pharmacokinetic/pharmacodynamic analysis. Responsibilities include developing robust mRNA-based bioanalytical capabilities, troubleshooting scientific issues, and collaborating with external partners. The position also offers opportunities to work with Generative AI and digital tools to enhance scientific workflows.

Moderna Oxford, United Kingdom

(Fixed-Term) GMP Engineering Specialist

This role involves providing engineering support for GMP manufacturing equipment, ensuring operability and reliability across process platforms. Responsibilities include troubleshooting, authoring technical documents, and leading small-to-medium sized projects. The position is hands-on and cross-functional, essential for mRNA manufacturing success.

Moderna

Senior GMP Maintenance Technician

This role involves hands-on maintenance and troubleshooting of GMP and non-GMP equipment in a new manufacturing facility. Responsibilities include equipment reliability, CMMS ownership, and collaboration with Engineering and QA on capital and reliability initiatives.

Moderna

Associate Director, CMC Regulatory Affairs, International

This role involves leading CMC regulatory strategies and submissions for international markets, with a focus on mRNA-based products across vaccines, oncology, and rare diseases. The individual will guide global regulatory compliance, interact with health authorities, and support manufacturing and quality teams through regulatory interpretation and change control. It requires deep expertise in CTD-format filings and a proactive approach to managing multi-therapeutic regulatory programs in a fast-paced environment.

Moderna

On-site Permanent