Biotechnology Jobs

• Opfikon, Switzerland
• 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 and internal statistical programmers, and supports departmental improvement initiatives.

SAS · R

• Oxford
• On-site
• Mid-level
• Permanent

Designs and runs evolution campaigns and selection schemes to optimise photosynthetic proteins, applying genome editing, directed evolution and protein engineering within a stage-gated plant engineering programme. Works in an interdisciplinary team translating photosynthesis, carbon fixation and yield findings into commercial and IP opportunities.

• Oxford
• On-site
• Mid-level
• Permanent

Designs and runs quantitative genetics experiments to assess polygenic traits in field environments, managing multi-location field sites and identifying germplasm for trait variation analysis. Works within the Photosynthesis and Yield programme, taking a plants-down approach to build discovery pipelines from natural variation and evolutionary signals, with scope to contribute to publications, IP and commercial translation.

• Hyderabad, India
• On-site
• Director · manages people

Acts as the primary interface between business stakeholders, biostatisticians, statistical programmers and technical delivery teams, translating clinical and statistical requirements into scalable R-based analytics, automation workflows and enterprise reporting. Leads requirement workshops, manages a small team, and oversees releases with end-to-end traceability, regulatory compliance and audit readiness across the clinical trial lifecycle.

• London
• Hybrid
• £67,900 – £126,100 pa
• Senior

Co-leads cross-functional Clinical Trial Teams and global studies from planning through close-out, managing timelines, budgets, risks and inspection readiness. Partners across global and local functions on recruitment, data operations and vendor performance, while championing operational excellence and continuous improvement.

• London
• Hybrid
• US$189,750 – US$316,250 pa
• Director

Leads precision diagnostics strategy for oncology programmes, defining diagnostic requirements for trials and overseeing biomarker selection, assay validation and sample handling. Manages project plans, budgets and timelines while engaging diagnostic companies, clinical labs and vendors, and supporting regulatory submissions. Works cross-functionally with research, clinical, regulatory and commercial teams in a hybrid model.

FDA · EU IVDR · PMDA +2

• Stevenage
• Hybrid
• Director

Leads precision diagnostics strategy for oncology programmes, defining biomarker selection, assay validation and sample collection across multiple assets. Oversees project plans, budgets and regulatory submissions while managing external diagnostic partners and clinical labs. Hybrid role based in Stevenage, relocating to Cambridge by early 2029.

FDA · EU IVDR · PMDA/MHLW Japan +2

• 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

• Newcastle upon Tyne
• £21,805 pa
• Entry level
• Contract

Investigates the molecular mechanisms of liver dysfunction in childhood POLG-related mitochondrial disease, focusing on Alpers-Huttenlocher syndrome. Uses quantitative untargeted proteomics and immunohistochemistry on donated post-mortem liver tissue, and generates hepatic organoids from patient-derived iPSCs for disease modelling and therapeutic screening. Based in the Newcastle Mitochondrial Research Group with a placement at the University of St Andrews.

iPSCs

• Cambridge
• Senior
• Permanent

Lead biophysical binding characterisation, predominantly using Surface Plasmon Resonance, to interrogate Bicycle® molecules and triage screening cascades. Design and optimise bespoke assays, explore orthogonal technologies such as Carterra, AlphaScreen and mass photometry, and partner with computational and structural biology teams on structure-based drug design. Mentors junior colleagues within the Platform Technology group.

SPR · Carterra · AlphaScreen +4

• London
• Remote
• Lead

Supports the Centralized Monitoring Lead in building study-specific monitoring strategies, programming quality tolerance limits, key risk indicators and data visualisations on the Cluepoints platform. Handles platform setup, scheduled refreshes, specification documents and peer reviews, working directly with a sponsor on a dedicated project. Requires strong SAS macro skills and prior data management experience.

Cluepoints · SAS · EDC Systems +1

• London
• Hybrid
• Senior
• Permanent

Architect novel generative models to design functional proteins, working in an interdisciplinary team of ML researchers, protein engineers and biologists. Split roughly 90/10 between building and evaluating models against wet lab results and self-development, with heavy emphasis on data pipelines, cloud training and production-quality code.

NeurIPS · ICML · ICLR

• London
• Remote
• Senior · manages people

Leads cross-functional clinical trial teams for biotech clients, owning project plans, budgets, P&L, risk management and client relationships from Phase I to III. Requires strong CRO experience and therapeutic expertise in oncology plus areas such as dermatology, women's health, neurology, rare disease or radiopharmaceuticals, working fully remotely within a select EMEA country.

Microsoft Excel · PowerPoint · Microsoft Word +1

• Newcastle upon Tyne
• On-site
• Entry level
• Permanent

Graduate-level role in a cancer diagnostics R&D team, generating and evaluating antibodies and detection methods for in vitro diagnostic assays on manual and automated staining systems. Involves laboratory work, literature and competitor reviews, and contributing to product development, verification and validation in a regulated environment, with training in histopathology and immunohistochemistry.

Automated Staining Systems · Manual Staining Systems

• Uxbridge
• Director

Leads medical monitoring and clinical development for neuroscience trials, overseeing safety reviews, protocol design, and site interactions. Partners with Clinical Scientists on study delivery and serves as medical expert in health authority interactions and publications. Requires deep disease-area expertise and industry clinical trial experience.