Biotechnology Jobs

• London
• On-site
• Director

Shape global CMC regulatory strategy for an innovative mRNA medicines portfolio, driving international submissions and health authority interactions. Prepare and review CMC sections of regulatory filings, advise Manufacturing and Quality teams, and oversee multiple development programs. An individual contributor role with global reach, working alongside teams using digital and Generative AI tools.

Generative AI

• Oxford
• Hybrid · 3–4 days in office
• Director

As an individual contributor in the Clinical Pharmacology group, you will develop quantitative strategies for dose selection, PK/PD characterization and regimen optimization across oncology, immunology and rare disease programs. You will partner with Pharmacometrics and QSP colleagues, represent CQP on program teams, and contribute to regulatory documentation and interactions.

R · Phoenix WinNonlin · NONMEM +2

• Leeds
• Director · manages people

Executive leadership role owning QA and regulatory compliance for the Clinical Pharmacology Services unit, covering CPU operations, GMP pharmacy activities and Phase IB/IIA early-phase trials. Sets risk-based quality strategy, inspection readiness and audit programs, leads global matrixed QA teams and represents the company externally on GCP/GMP matters.

• Oxford
• On-site
• £40,000 pa
• Senior
• Permanent

Develops and optimises LC-MS workflows for low-input and single-cell proteomics and/or metabolomics, supporting researchers across the institute with experiment design, method development, data acquisition and interpretation. Works closely with bioinformatics, scientific computing and AI/ML teams, and helps build SOPs and training material for single-cell MS capability.

LC-MS · Flow Cytometry · Sequencing +5

• Maidenhead
• Hybrid · 3 days in office
• US$212,000 – US$251,000 pa
• Director

Leads the full statistical contribution to a clinical development programme, defining statistical strategy for trial design, analysis and regulatory submissions, and representing Biostatistics in interactions with the FDA, EMA and PMDA. Also manages outsourcing to CROs/FSPs and contributes to governance and development-plan decisions across therapeutic areas.

SAS · R

• Breda, Netherlands
• Hybrid · 3 days in office
• US$212,000 – US$251,000 pa
• Director

Leads the full scope of statistical contribution to a clinical development programme, defining statistical strategy and methodologies for trial design, analysis and regulatory submissions. Represents Biostatistics in interactions with authorities such as FDA, EMA and PMDA, and manages outsourcing or internal statistical programmers. Two positions support multiple therapeutic areas.

SAS · R

• Oxford
• On-site
• £40,000 pa
• Entry level
• Permanent

Postdoctoral role in the Liu Lab for Synthetic Evolution, designing and troubleshooting experiments, analysing complex data with computational and statistical tools, and publishing high-quality research. The lab invented OrthoRep for continuous accelerated gene evolution, with projects spanning antibody sequence-affinity datasets, enzyme sequence-function maps, and de novo gene function emergence. Involves mentoring junior researchers and collaborating across multidisciplinary teams.

OrthoRep

• London
• Hybrid
• €63,600 – €118,000 pa
• Lead · manages people

Lead and develop a team of Central Monitors while shaping risk-based monitoring strategies across a global clinical development portfolio. Oversee trial-data surveillance, signal detection and Key Risk Indicators, translating complex risk signals into actionable insights for Clinical Trial Teams. Works in a global matrix with clinical, data and risk-surveillance teams, driving continuous improvement through analytics and technology.

Artificial Intelligence

• Dublin, Ireland
• Hybrid
• €63,600 – €118,000 pa
• Lead · manages people

Lead and develop a team of Central Monitors while shaping risk-based monitoring strategies across a global clinical development portfolio. Oversee trial-data surveillance, signal detection and insight generation, translating complex risk signals into actionable insights and designing study-specific Key Risk Indicators and Quality Tolerance Limits.

Artificial Intelligence

• Waltham, United States
• Hybrid · 2–3 days in office
• US$151,500 – US$252,500 pa
• Director

Leads cross-functional project teams within Oncology Translational Medicine, coordinating diagnostics, biomarker, clinical development, regulatory and finance activities across internal groups and external partners. Manages integrated timelines, budgets, contracts and invoices, tracks milestones and risks, and supports regulatory documentation and technical evaluations of diagnostic technologies.

Microsoft Project · Microsoft Word · Microsoft Excel +7

• Stevenage
• Hybrid · 2–3 days in office
• US$151,500 – US$252,500 pa
• Director

Leads cross-functional project teams within Oncology Translational Medicine to progress diagnostic and biomarker development activities, coordinating with clinical, regulatory, quality, finance and external lab partners. Builds integrated timelines, tracks budgets, milestones and contracts, mitigates risks, and supports regulatory submissions and technical evaluations of diagnostic technologies.

Microsoft Project · Microsoft Word · Microsoft Excel +7

• Welwyn
• On-site
• Lead · manages people

Drives and facilitates efficient study start-up for Roche-sponsored clinical trials across the UK, developing start-up strategies and overseeing site activation and regulatory compliance. Engages with Ethics Boards, Health Authorities and CROs, manages budgets and contracts, and champions process automation and team development.

REC · MHRA · HRA

• London
• Hybrid · 3 days in office
• Lead

Technically lead the Platform group, owning cloud infrastructure and the software lifecycle for training and inference systems. Work across GCP, Kubernetes, Docker and Terraform with scientists and ML researchers, reporting to the Director of Engineering in a small, fast-moving team.

GCP · Kubernetes · Docker +7

• London
• Hybrid · 3 days in office
• Senior

Lead the hardening and scaling of an inference platform serving fleets of cutting-edge ML models for scientific applications. Set strategy and roadmaps, architect next-generation services to solve scaling limits, and partner with research, product and operations teams to align infrastructure with biotech R&D cycles.

Kubernetes · Google Cloud Platform · NVIDIA GPU +1

• Macclesfield
• On-site
• Senior
• Permanent

Perform routine and non-routine analytical testing of pharmaceutical oral drug products and new modalities using HPLC, Karl Fischer, dissolution and mass spectrometry. Review data for GLS and GMP compliance, investigate out-of-specification results, and develop, optimise and validate analytical methods while training colleagues and driving continuous improvement at a client's Macclesfield facility.

HPLC · Karl Fischer · Mass Spectrometry +1