Latest Biotech Research Scientist Jobs

Senior Software Engineer (Inference Platform), London

This role involves leading the reliability and scalability of AI/ML infrastructure for biotech applications, focusing on GPU/TPU systems, workload orchestration, and inference services. The engineer will overhaul monitoring, improve CI/CD stability, and ensure robust platform performance to support cutting-edge drug discovery research. Close collaboration with research and applied ML teams is central to the role.

Isomorphic Labs London, United Kingdom

On-site Permanent

Software Engineer (Compute Platform), London

This role involves designing and managing large-scale GPU/TPU infrastructure to support cutting-edge AI-driven drug discovery. You'll work closely with machine learning and research teams to optimize hardware performance, deploy Kubernetes-based systems, and scale compute platforms across cloud environments. The position focuses on building reliable, high-performance infrastructure for AI workloads in a biotech context.

Isomorphic Labs London, United Kingdom

On-site Permanent

Associate Director, Clinical Trial Disclosure & Transparency

This role leads global clinical trial disclosure and transparency strategy, ensuring compliance with international regulations such as FDAAA, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while guiding cross-functional teams and managing vendor performance. They also support redaction of confidential information and drive process improvements across disclosure operations.

CSL United Kingdom

Associate Director, Global Regulatory Science, CMC

Leads global regulatory strategy for CMC (Chemistry, Manufacturing, and Controls) in support of mRNA-based medicines, ensuring compliance with international regulations and guiding submissions across multiple therapeutic areas. Works closely with manufacturing, quality, and development teams to prepare high-quality regulatory documentation and engage with health authorities. Focuses on biologics, particularly in vaccines, oncology, and rare diseases, within a rapidly expanding biotech environment.

Moderna London, United Kingdom

Hybrid Permanent

Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading scientific strategy and execution for immunogenicity and ligand binding assays 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 regulatory standards. The position emphasizes data integrity, cross-functional collaboration, and integration of emerging technologies, including AI-enabled data analysis, to accelerate clinical development.

Moderna Oxford, United Kingdom

Hybrid Permanent

Senior Computational Biologist - Early Discovery Oncology

Drive target discovery and validation in precision oncology by integrating multimodal biological data (phenomics, transcriptomics, genomics, proteomics) to identify novel therapeutic targets. Collaborate with cross-functional teams to develop scalable computational methods and build compelling data packages that advance drug programs. Develop criteria for target nomination and support early translational strategies using AI-powered platforms.

Recursion United Kingdom £151,800 – £220,660 pa

Hybrid Permanent

Quality Engineer - Medical Devices - Didcot

Quality Engineer - Medical Devices - DidcotA pioneering medical device company in Didcot is looking to appoint a Quality Engineer to support the continued development, manufacture and improvement of its life‑changing technology. Newton Colmore is recruiting for this position exclusively,...

Newton Colmore Didcot, Oxfordshire, United Kingdom

Metabolite Identification Specialist

This role involves leading metabolite identification and biotransformation studies to determine the metabolic fate of drug candidates. The specialist will design and interpret advanced analytical data using techniques like high-resolution mass spectrometry, support drug discovery and development programmes, and provide scientific guidance to project teams and junior scientists. The position emphasizes technical leadership, problem-solving in complex metabolic pathways, and direct contribution to the progression of pharmaceutical candidates.

SRG Sandwich, United Kingdom

On-site Permanent

GMP Production Manager

Lead cleanroom production operations in a GxP-regulated environment, ensuring compliance with quality and safety standards while managing equipment, workflows, and cross-functional collaboration. Oversee manufacturing processes, support audits and validations, and drive continuous improvement within a science-led, patient-focused organisation.

VRS Recruitment Wiltshire, United Kingdom

On-site Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK's global assets, with a focus on safety evaluation and benefit-risk management across clinical development and post-marketing settings. The position requires expert analysis of clinical and safety data, leadership in cross-functional governance teams, and strategic input into regulatory submissions and risk mitigation. It plays a critical part in ensuring patient safety and regulatory compliance within immunology and other therapeutic areas.

GSK United States US$169,950 – US$283,250 pa

On-site Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK’s global assets, with a focus on immunology. The Scientific Director will evaluate safety data, lead cross-functional teams, and ensure compliance in clinical development and post-marketing settings. The position requires deep expertise in safety evaluation, signal detection, and international regulatory standards.

GSK US$169,950 – US$283,250 pa

On-site Permanent

Senior Manager, Clinical Operations - FSP Resource & Vendor Management

This role leads the strategic management of Functional Service Provider (FSP) resources within Clinical Operations, shaping workforce planning, vendor performance, and financial oversight. The individual will develop data-driven resourcing models, act as the primary Clinical Operations liaison to FSP vendors, and ensure alignment with procurement and finance functions. It involves governance, system optimization, and advisory support to clinical leaders, with a focus on cost, quality, and scalability in a global matrix environment.

CSL US$170,000 – US$201,000 pa

Hybrid Permanent