Jobs in Stoke-on-trent

ViiV Healthcare (GSK) Medical Director, ViiV R&D Physician Center of Excellence

The Medical Director role at ViiV Healthcare focuses on managing and overseeing Phase 1-4 clinical trials, ensuring the successful planning, execution, and reporting of protocols. Key responsibilities include providing medical governance, managing safety events, and collaborating with internal and external stakeholders to develop groundbreaking HIV treatments.

GSK

On-site Permanent

ViiV Healthcare (GSK) Statistics Leader

The Statistics Leader at ViiV Healthcare will provide statistical leadership and support for one or more HIV treatment programs. Responsibilities include managing statistical contributions, influencing project strategies, and ensuring the scientific integrity of data dissemination. The role involves cross-functional collaboration, advanced analytics, and mentoring team members.

GSK

On-site Permanent

(Fixed Term) Analyst, Quality Control, Chemistry & Stability

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna Oxford, United Kingdom

(Fixed Term) Analyst, Quality Control, Chemistry & Stability

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna Gargrave, BD23 3RZ, United Kingdom

Principal Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves leading high-parameter spectral flow cytometry activities in a GCLP-compliant clinical laboratory, generating immunophenotyping and functional immune profiling data from PBMC and whole blood samples to support mRNA-based clinical development. The scientist will independently execute and analyze complex assays, contribute to assay development and validation, and ensure regulatory compliance while leveraging advanced platforms like the Cytek Aurora. Opportunities exist to engage with digital tools and generative AI for data interpretation and workflow optimization within a collaborative, innovation-driven environment.

Moderna Oxford, United Kingdom

Hybrid Permanent

Scientist, Clinical Biomarker Laboratory, Immuno-Assays - Cell Based

This role involves leading the development, qualification, and validation of cell-based immunoassays to support Moderna’s clinical trials across multiple therapeutic areas. The scientist will generate high-quality, GLP/GCP-compliant data from clinical samples, contribute to regulatory documentation, and collaborate with cross-functional teams and external partners. Emphasis is placed on scientific rigor, innovation in assay design, and mentoring junior staff within a regulated, collaborative laboratory environment.

Moderna Oxford, United Kingdom

Hybrid Permanent

Senior Research Associate, Clinical Biomarker Laboratory, Immunoassays

This role involves hands-on development, qualification, and validation of functional immunoassays to support mRNA-based clinical trials. The scientist will conduct experiments, analyze data, and ensure regulatory compliance in a GCP environment, contributing directly to patient-impacting therapeutics across multiple disease areas.

Moderna Oxford, United Kingdom

Hybrid Permanent

Senior Automation Engineer, Laboratory Automation & Biobanking

This role involves designing and optimizing automated workflows for clinical biomarker assays using advanced liquid handling systems and Hamilton platforms. The engineer will integrate automation with data systems like LIMS, develop AI-enhanced laboratory workflows, and ensure compliance with GLP/GCLP standards. A key focus is building scalable, digitally connected laboratory ecosystems to support high-throughput sample management and biobanking operations.

Moderna Oxford, United Kingdom

Hybrid Permanent

Associate Director, CMC Regulatory Affairs, International

This role involves developing and implementing CMC regulatory strategies for international submissions, providing guidance on regulatory CMC aspects, and leading discussions with health authorities. The candidate will also support the creation of CMC submission templates and offer interpretations of regulatory guidance documents, ensuring compliance and efficient delivery of high-quality regulatory documentation.

Moderna London, United Kingdom

On-site Permanent

Senior Project Specialist, Clinical Supplies

This role involves managing end-to-end clinical supply operations for Moderna’s mRNA-based therapies, ensuring investigational products are labeled, packaged, and distributed efficiently and in compliance with regulatory standards. The specialist coordinates with CROs, vendors, and internal teams to maintain supply chain continuity, troubleshoot logistics, and support digital innovation in supply systems, including AI-enabled tools and IRT platforms.

Moderna

Hybrid Permanent

Sr. Engineer, Process Automation

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.As Moderna continues to expand its presence in Harwell, this role...

Moderna

Manager, Global Regulatory Science CTA

This role involves leading the operational execution of Clinical Trial Applications (CTAs) globally, outside the US, with a focus on the UK regulatory landscape. Responsibilities include managing CTA submissions, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.

Moderna Poland

On-site Permanent

Manager, Global Regulatory Science CTA

This role involves leading the operational execution of Clinical Trial Applications (CTAs) globally, outside the US, with a focus on the UK regulatory landscape. Responsibilities include managing CTA activities, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.

Moderna

On-site Permanent

Principal Scientist, Bioanalytical & Molecular Assays

This role involves leading the development and validation of advanced molecular assays (including RT-qPCR, dPCR, and NGS) to support clinical biomarker programs across Moderna’s therapeutic pipeline. The scientist will drive end-to-end assay lifecycle management, ensure regulatory compliance with GCLP standards, and collaborate with cross-functional teams to generate high-quality genomic data for clinical decision-making. Emphasis is placed on innovation, data integrity, and integrating emerging technologies like AI-enabled tools to accelerate translational research.

Moderna

Hybrid Permanent

Principal Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves generating and analyzing high-parameter flow cytometry data from clinical trial samples to support immunology research in a GCLP-compliant environment. The scientist will operate advanced spectral flow platforms like the Cytek Aurora, perform ex vivo immune functional assays, and ensure data integrity through rigorous documentation and compliance. Emphasis is placed on innovation through AI-enabled tools, assay development, and mentoring within a collaborative, regulated laboratory setting.

Moderna

Hybrid Permanent