Latest Research Scientist Jobs

Bioinformatics Engineer

The role involves building and maintaining scalable bioinformatics data infrastructure and workflow orchestration systems to support plant science research. You will develop Nextflow pipelines, ETL processes, and reproducible workflows that integrate omics data from lab instrumentation into analysis-ready formats. Collaboration with bioinformaticians, data analysts, and systems administrators ensures solutions meet evolving research needs in a high-performance computing and cloud environment.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

Bioinformatician - Pathogen

This role involves developing and refining bioinformatics workflows to analyse whole genome and metagenomic sequencing data for infectious disease diagnostics. The bioinformatician will work closely with wet lab scientists to interpret complex datasets, focusing on taxonomic classification, antimicrobial resistance prediction, and strain characterisation. The position supports a translational research initiative aiming to deploy scalable diagnostic tools globally.

Ellison Institute of Technology Oxford, United Kingdom

Hybrid Permanent

Field Service Engineer, Medical Diagnostic Systems

This role involves servicing and repairing advanced medical diagnostic systems in NHS and private laboratory settings, including on-site troubleshooting and breakdown response. The engineer will work with high-value, complex equipment and provide technical solutions directly to laboratory staff. Full product training is provided, and the role requires a flexible schedule with some weekend work.

TRS Consulting Portsmouth, Hampshire, United Kingdom £52,000 pa

Field Service Engineer, Medical Diagnostic Systems

This role involves servicing and repairing advanced medical diagnostic systems in NHS and private laboratory settings. The engineer will perform on-site maintenance, troubleshoot technical issues, and deliver customer support across pathology and clinical chemistry departments. Full product training is provided, and the role requires a flexible schedule including weekend work.

TRS Consulting Poole, Dorset, United Kingdom £52,000 pa

Clinical Development Senior Medical Director - Vascular

Leads clinical development for vascular programmes across early and late phases, shaping study designs and clinical development plans. Works cross-functionally with translational science, regulatory, and commercial teams to advance medicines for vascular disease, with a focus on patient impact and scientific innovation. Provides medical oversight, contributes to regulatory submissions, and guides decision-making in a matrix environment.

GSK Stevenage, United Kingdom

Medical Director Clinical Development- Aging

This role involves leading clinical development for aging-related research within GSK’s Respiratory, Immunology & Inflammation unit. The Medical Director will design and execute clinical development plans, provide medical oversight, and integrate translational and clinical data to advance drug candidates. The position emphasizes cross-functional leadership, regulatory engagement, and innovation in addressing unmet needs in aging and immune science.

GSK United States £189,750 – £316,250 pa

Trial Master File Oversight Manager

This role involves overseeing the quality and completeness of global Trial Master Files (TMF) for clinical trials, ensuring compliance and audit readiness. The manager will lead vendor oversight, identify documentation risks, drive remediation, and support continuous improvement in TMF processes. Collaboration with cross-functional teams and stakeholders is central to maintaining high standards in clinical documentation.

Novartis London, United Kingdom £49,140 – £91,260 pa

Hybrid Permanent

Global Labelling Manager, Content (Neuroscience)

This role involves leading the development and maintenance of global core labelling documents for neuroscience products, ensuring accuracy, compliance, and consistency across markets. The individual will facilitate cross-functional alignment, conduct competitor and regulatory research, and support implementation of labelling updates throughout the product lifecycle. Collaboration with regulatory, clinical, and safety teams is central to maintaining high-quality, audit-ready documentation.

Novartis

Hybrid Permanent

Clinical Development Senior Medical Director - Vascular

Lead clinical development for vascular programs across early and late-phase trials, designing studies and translational plans to advance medicines for cardiovascular disease. Collaborate with cross-functional teams to shape clinical strategies, ensure regulatory compliance, and drive patient-focused innovation within GSK’s R&D pipeline.

GSK

Clinical Development Senior Medical Director - Vascular

Lead clinical development for vascular programmes across early and late phases, designing studies and translational plans to advance medicines for cardiovascular disease. Collaborate with cross-functional teams to shape clinical strategies, ensure patient safety, and drive innovation in drug development. Play a key role in regulatory interactions, trial oversight, and identifying transformative opportunities in vascular medicine.

GSK

Clinical Development Senior Medical Director - Vascular

Lead clinical development for vascular programmes across early and late-phase studies, shaping clinical plans and study designs to accelerate safe, meaningful medicines for vascular disease. Work cross-functionally with translational science, regulatory, safety, and commercial teams to deliver clinical development strategies and drive innovation in cardiovascular medicine.

GSK

Associate Director of Clinical Sciences

Lead clinical sciences strategy and execution for global oncology studies, with responsibility for end-to-end protocol development, clinical data review, and cross-functional collaboration. Focus on immuno-oncology with strong emphasis on regulatory compliance, patient safety, and scientific leadership across clinical development phases. Work within a matrix environment to guide study design, interpretation, and regulatory submissions.

GSK Stevenage, United Kingdom

Associate Director of Clinical Sciences

This role involves leading clinical sciences activities in global oncology studies, with responsibility for end-to-end protocol development, clinical data review, and cross-functional collaboration. The individual will shape study design, interpret results, and ensure regulatory compliance across phases of development, with a focus on immuno-oncology. The position requires scientific leadership, engagement with external experts, and contribution to regulatory submissions and clinical strategy.

GSK United States

Associate Director of Clinical Sciences

This role involves leading clinical sciences activities within global oncology R&D, focusing on study design, protocol development, and clinical data review across the development lifecycle. The individual will act as a subject matter expert, ensuring scientific rigor and regulatory compliance while collaborating with cross-functional teams and external partners. A key focus is on immuno-oncology, with responsibilities spanning from early-phase to late-stage clinical development.

GSK

VP, Medicine Development Leader - Specialty Product Development

This role leads the global development of a medicine from clinical proof of concept to first-market approval, serving as the single point of accountability within GSK's matrixed R&D environment. The VP Medicine Development Leader will build and lead a cross-functional team, define strategic development plans, and ensure alignment with regulatory, commercial, and manufacturing stakeholders. The position emphasizes evidence-based decision-making, lifecycle planning, and patient-focused development across multiple indications.

GSK Stevenage, United Kingdom £242,250 – £403,750 pa