Biotechnology Jobs

• London
• Hybrid · 3 days in office
• Lead

Build and evolve a large-scale ML infrastructure platform that supports training and deploying novel models across vast compute and data pools. Work cross-functionally with research, engineering and product teams, exploring agent deployment and distributed, performance-critical workloads. Hybrid role in London requiring three office days a week.

Kubernetes · Google Cloud Platform · GCP +1

• London
• Hybrid · 3 days in office
• Senior

Join a newly formed LLM Engineering team to architect, build and own scalable, secure infrastructure bringing large language models into scientific and business workflows. Work spans system design, agentic tooling, RAG, evaluation frameworks and fine-tuning, partnering closely with AI researchers and drug discovery experts.

vLLM · MCP · GCP

• Oxford
• On-site
• Entry level
• Temporary

Support assay development, qualification, validation and clinical sample testing within Moderna's Immunoassay group, generating bioanalytical data that informs clinical trials. Work is primarily lab-based (≥85% of time) under a study lead, with responsibility for data integrity, reagent preparation, equipment upkeep and compliance with GCP/ISO standards.

GraphPad Prism · LIMS · Word +2

• Oxford
• On-site
• Senior

Leads the creation, review and oversight of investigator site budgets and grants across Phase I–IV clinical trials, using Grants Manager/GrantPlan and FMV benchmarking. Manages CRO site budget and CTA negotiations, scenario planning and site activation timelines, with exposure to Generative AI tools for analytics.

Grants Manager · GrantPlan · MS Office +1

• London
• Hybrid · 2–3 days in office
• Mid-level

Lead advanced analytics projects within ViiV's Medical function, translating strategic priorities into analytical approaches, measurement frameworks and actionable insights. Build models, oversee dashboard design with vendors, and advance AI/ML and agentic workflows across Medical Analytics while partnering with Commercial, Digital and Data Governance teams.

Python · R · SQL +1

• Stevenage
• Hybrid
• Director

Leads acquisition, integration and analysis of large-scale cancer multi-omic and clinical datasets to drive translational decisions and support the oncology pipeline. Partners with biologists, clinicians, AI/ML engineers and statisticians, building reproducible data pipelines and informatics infrastructure, with mentoring responsibilities in a hybrid team.

Cloud Platforms

• Aberystwyth
• £27,319 – £30,378 pa
• Contract

Supports a Wellcome-funded schistosomiasis drug discovery programme, working within a collaborative team across Aberystwyth, Dundee and UT Southwestern. The role involves in vivo animal work underpinning phenotypic and target-based screening of new chemical entities against parasitic trematode worms.

• Reading
• Mid-level · manages people

Leads end-to-end delivery of regional and global clinical trials embedded within a sponsor's team, managing timelines, budgets, risk and cross-functional groups. Also supports bid defence presentations, vendor management and financial forecasting, mentoring less experienced project team members.

IQVIA

• Manchester

Field-based role selling laboratory reagents and custom/bulk chemicals directly to customers and through top-tier distributors across Northern UK. You build territory plans, forecast, maintain CRM, train sales reps, and support trade shows, working with clients in pharma, food and beverage, and environmental testing. Requires a chemistry background and frequent travel.

CRM

• Cardiff
• Lead

Develops and drives the long-term global operations and supply chain footprint strategy for the Discovery & Medical business, translating business strategy into network and footprint roadmaps across manufacturing, sourcing, warehousing, capacity, localization and productivity. Leads business-case development, CapEx/OpEx planning and governance for cross-functional footprint initiatives, with up to 30% international travel.

Danaher Business System · Automation · Additive Manufacturing

• Reading
• Lead

Provides principal-level statistical leadership across Phase II and III clinical trials, independently leading SAP authoring and review while supporting integration activities across studies and programmes. Acts as a proactive statistical partner to clinical, programming and regulatory teams, ensuring compliant, high-quality outputs are delivered on time. Requires strong R programming and immunology therapeutic area exposure is desirable.

R

• Saffron Walden
• Hybrid
• £3,452 – £3,861 pm
• Contract

Curate molecular interaction and macromolecular complex data from scientific literature and user depositions into the IntAct and Complex Portal knowledgebases. Work with bioinformaticians and developers to build curation workflows combining expert manual curation with AI-assisted literature mining, using ontologies and community data standards.

IntAct · Complex Portal · Gene Ontology +2

• Saffron Walden
• Hybrid · 2 days in office
• £4,395 pm
• Lead · manages people
• Contract

Lead the scientific data programme behind FENIX, a unified platform for archiving and exploring functional genomics datasets. You will line manage bioinformaticians and curators, own data standards and quality controls, and guide reproducible Nextflow workflow development while acting as principal scientific liaison with teams such as ENA, Ensembl and UniProt.

Nextflow · Python · R +7

• Oxford
• Hybrid
• Entry level
• Internship

A 12-month industrial placement within a biotechnology company's community affairs team, based at an Oxford learning lab dedicated to STEAM education. The role involves developing and delivering hands-on science lessons with local schools, preparing lab materials and reagents, managing supplies, and supporting volunteers and scientists. It combines science communication and outreach with practical lab and administrative duties.

• London
• Remote
• Mid-level

Oversees medical coding activities across clinical studies, managing coding dictionaries such as MedDRA and WHODrug, reviewing coded data for accuracy and compliance, and preparing coding reports for medical review. Acts as subject matter expert, delivering training and partnering with Clinical Development, Pharmacovigilance and Data Management teams to drive process improvements and regulatory compliance.

MedDRA · WHODrug