Latest Healthcare Jobs

Microbiology Industrial Placement, 2027

This industrial placement in microbiology at GSK offers hands-on experience in a pharmaceutical laboratory, focusing on quality control, environmental monitoring, and compliance. You'll work on real projects, learn key laboratory techniques, and contribute to continuous improvement initiatives.

GSK United Kingdom

Pharmaceutical Science (Multiple Roles and Locations) Industrial Placement, 2027

This industrial placement at GSK offers hands-on experience in pharmaceutical manufacturing, quality control, and process improvement across multiple sites. You'll work on real projects, learn from experienced professionals, and gain valuable skills in GMP, data analysis, and technical troubleshooting.

GSK United Kingdom

Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading and executing phase-appropriate bioanalytical strategies for immunogenicity and ligand binding assays (LBA) within Moderna’s mRNA-LNP therapeutic pipeline. The Principal Scientist will oversee assay development, validation, and sample analysis, ensuring regulatory compliance and scientific rigor across clinical programs. The position emphasizes collaboration with cross-functional teams, integration of emerging technologies including AI-enabled tools, and contribution to regulatory submissions and data interpretation in a GcLP-compliant environment.

Moderna Oxford, United Kingdom

Hybrid 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

Associate Director, Associate Clinical Operations Asset Lead (aCOAL)

This role involves leading and supporting the operational strategy and delivery for late-phase oncology clinical trials. Responsibilities include coordinating cross-functional inputs, maintaining inspection readiness, and contributing to protocol development and regulatory deliverables. The role offers opportunities for career growth and strategic influence within GSK's clinical operations team.

GSK

Associate Director, Associate Clinical Operations Asset Lead (aCOAL)

This role involves leading and supporting the operational strategy and delivery for complex oncology clinical trials, ensuring alignment with the clinical development plan. Responsibilities include coordinating cross-functional inputs, maintaining inspection readiness, and providing operational input for regulatory deliverables.

GSK

Associate Director, Associate Clinical Operations Asset Lead (aCOAL)

This role involves leading and supporting the operational strategy and delivery for complex oncology clinical trials, coordinating cross-functional inputs, and maintaining inspection readiness. The position offers opportunities for growth and influence over program strategy.

GSK

Associate Director, Associate Clinical Operations Asset Lead (aCOAL)

This role involves leading and supporting the operational strategy and delivery for complex oncology clinical trials, coordinating cross-functional inputs, and maintaining inspection readiness. The position offers opportunities for growth and influence over program strategy.

GSK

Senior Research Associate, Bioanalytical & Molecular Assays

This role involves developing, optimizing, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and RNA isolation—to support mRNA-based clinical programs. The scientist will work within GCL0-compliant (GCLP) frameworks to generate pharmacokinetic and pharmacodynamic data, ensuring regulatory compliance and data integrity. Collaboration with cross-functional teams and adoption of digital tools and automation are key to advancing clinical trial execution and analytical processes.

Moderna

Hybrid Permanent

Sr. Manager, Site Budgets and Contracts

This role involves leading the creation and management of investigator site budgets and contracts for global clinical trials, using Grants Manager and FMV benchmarking tools. The Senior Manager collaborates with CROs, Legal, and Clinical Operations to ensure site budgets align with study forecasts and are executed on time. Responsibilities include strategic planning, contract negotiation oversight, risk identification, and process improvement within an outsourced trial model.

Moderna

Hybrid Permanent

Principal Scientist, Bioanalytical & Molecular Assays

This role involves leading the development and validation of advanced molecular assays—including RT-qPCR, dPCR, and NGS-based methods—for clinical biomarker programs at Moderna. The scientist will drive end-to-end assay lifecycle management, ensure compliance with GCLP and regulatory standards, and collaborate across multidisciplinary teams to generate high-quality genomic data. A key focus is integrating genomics, bioinformatics, and clinical insights to support drug development and inform future pipeline strategies.

Moderna

Hybrid Permanent

Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading scientific strategy and execution for immunogenicity and ligand binding assays (LBA) in support of Moderna’s mRNA-LNP therapeutic programs. The Principal Scientist will oversee regulated bioanalytical activities including assay development, validation, and sample analysis, ensuring compliance with GcLP, GLP, and GCP standards. The position plays a key role in clinical development by generating high-quality data to inform regulatory submissions and advance innovative medicines, with opportunities to engage in AI-enabled and digital analytical approaches.

Moderna

Hybrid Permanent

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

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

(Fixed Term) Scientist, Immunogenicity, Bioanalytical and Molecular Assays

This role involves designing and executing bioanalytical and immunogenicity strategies to support mRNA-based clinical development programmes. The scientist will lead assay development—including ADA, nAb, PK, and PD assays—using platforms like ELISA, MSD, and cell culture, while ensuring regulatory compliance and contributing to Moderna's expanding capabilities in Harwell. The position emphasizes collaboration across multidisciplinary teams and integration of digital and AI-enabled tools to enhance data interpretation and decision-making.

Moderna

On-site