Biotechnology Jobs

• Stevenage
• Hybrid · 2–3 days in office
• Senior

Embedded with CMC business teams, you take high-priority AI use cases from problem framing to working prototypes at days-to-weeks cadence, then ship first production versions. The work centres on document authoring and generation for regulatory filings, building agentic and RAG pipelines, human-in-the-loop review workflows, and LLM evaluation with golden datasets and regression testing.

Claude Code · GitHub Copilot · Databricks AI Assistant +5

• London
• Hybrid
• Director · manages people

Leads GSK's Forward Deployed Engineering function for CMC R&D, setting strategy, hiring and mentoring engineers, and owning senior BU sponsor relationships. Personally contributes to strategic engagements building digital twins, physical AI and self-driving lab capability, using AI coding agents as the primary development mode.

Claude Code · GitHub Copilot · Databricks AI Assistant +3

• United Kingdom
• Hybrid
• Mid-level

Manages end-to-end clinical trial supply chains, developing study-specific plans, coordinating cross-functional teams, and ensuring GxP-compliant distribution and inventory levels. Represents the department externally, mentors junior staff, and drives process improvements within a global clinical supplies team.

Microsoft Office

• Saffron Walden
• Hybrid · 1–2 days in office
• £3,452 pm
• Mid-level
• Contract

Develops the user-facing Europe PMC service, building fast, accessible interfaces for searching and navigating a corpus of over 47 million biomedical publications. Works with UX, product, back-end and data science colleagues to create reusable components, integrate REST APIs and JSON data, and improve performance, accessibility and maintainability within an Agile team.

React · Vue · Git +2

• Oxford
• On-site
• £35,681 – £37,388 pa
• Entry level
• Contract

Conducts molecular virology research on virus-host cell interactions, focusing on cellular oxygen sensing and viral replication, under Dr Peter Wing. Involves viral culture at containment levels 2 and 3, CRISPR/siRNA screens, live-cell imaging, and lab management. Fixed-term, full-time post funded by ARIA.

R · Python · FIJI +7

• London
• Hybrid
• Lead

Leads statistical work for post-marketing clinical trials, observational studies and real world data investigations, serving as Statistics lead on assigned projects. Develops protocols, analysis plans and TFL specifications, collaborating with clinical development, medical affairs, health economics and real world evidence teams. Requires strong SAS and R skills with a drug developer mindset.

SAS · R

• Oxford
• On-site
• £39,424 – £47,779 pa
• Entry level
• Contract

Develop novel statistical and machine learning methods for large-scale genomic, phenotypic and health data, covering areas such as genomic language models, multimodal and federated learning, and multi-ancestry methods. Implement reproducible research software, apply it to biobank-scale datasets, evaluate statistical and predictive performance, publish findings and guide junior researchers.

• Saffron Walden
• Hybrid
• £38,570 – £49,893 pa
• Senior
• Contract

Develop and apply statistical and deep learning methods to cell-free DNA from pregnant women, calling fetal and maternal genotypes from high-coverage sequence data and building methylation-aware biomarkers for pregnancy complications. Work spans methods development, large cohort application and collaboration with international partners in a statistical genomics group.

Python · R · Unix +6

• London
• Remote
• Mid-level

Manages a portfolio of clinical research studies end to end, leading cross-functional teams and client relationships for Patient Cloud products such as eCOA/ePRO, eConsent and virtual trials. Involves risk assessment, study documentation and milestone tracking, with flexibility needed to work American time zones.

MS Office Suite · Google Workspace

• Lisburn
• On-site
• Entry level
• Internship

A 12–14 month university placement for penultimate-year students, supporting the Statistical Programming group on clinical trials. Day to day you produce analysis and submission datasets, statistical tables, graphs and data listings using SAS, while learning about the pharmaceutical industry, clinical trial conduct and good clinical practice within a global project team.

SAS · R · MATLAB +1

• Harrow
• Remote
• Mid-level

Independently leads statistical aspects of low-to-moderate complexity clinical trials, developing complex analysis strategies and executing them with SAS or R. Reviews analysis datasets, quality-controls statistical deliverables, and contributes to trial design, analysis plans, and regulatory submissions. Works within global cross-functional teams, liaising with clients on data analysis, scope, and budget.

SAS · R

• United Kingdom
• Remote
• Lead

Lead medical writer dedicated to a single client, authoring and reviewing clinical study reports, protocols, IBs, INDs and MAAs while advising on document strategy and regulatory requirements. Provides senior review, mentoring and training to junior writers and program managers, and leads process improvement initiatives. Therapeutic experience in neurology, immunology, oncology or vaccines is valued.

• London
• Hybrid
• Senior

Plans and executes medical and scientific engagement activities such as advisory boards, congress symposia, external expert engagements and medical education programmes across oncology, cardiovascular, renal, neuroscience and immunology. Works within the International Medical Affairs Center of Excellence, translating engagement strategy into operational plans, managing vendors, logistics and budgets, and reinforcing compliant, audit-ready ways of working.

CRM Software

• London
• Hybrid
• Senior

Leads global clinical data transparency and disclosure across registries and regulatory platforms such as CTIS, EMA Policy 0070 and Health Canada PRCI, acting as subject matter expert for assigned therapeutic areas. Manages vendor partnerships, FOI access requests, redaction and lay summary work, plus SOP governance, compliance reporting and audit readiness within Global Regulatory Affairs Excellence.

CTIS · ClinicalTrials.gov · EU Clinical Trial Register +3

• Oxford
• On-site
• Senior · manages people

Lead development, qualification, validation and execution of complex cell-based immunoassays generating clinical trial data across therapeutic areas. Act as scientific point of contact within the Immuno-assays group, performing GCP/GLP-compliant sample testing, authoring validation reports, and mentoring junior lab staff. Fully onsite at Harwell, reporting to the Associate Director, Immuno-assay UK.

GraphPad Prism · Microsoft Word · Microsoft Excel +2