Biotechnology Jobs

• Harrow
• Remote
• Senior · manages people

Senior Statistical Programmer role focused on R programming for clinical trial analysis and reporting, producing and QCing SDTM/ADaM datasets, tables, figures and listings. The position can act as Statistical Programming Lead, coordinating global teams, managing timelines and budgets, and liaising with sponsors and biostatistics. Dedicated to a single sponsor within an FSP model across UK, Poland, Serbia and Hungary.

R · SDTM · ADaM +1

• Stevenage
• Hybrid
• Lead

Owns operational delivery of diagnostics across early and late-stage oncology trials, covering biosample collection, processing and storage, and implementation of clinical trial assays at reference and central labs and CROs. Works in a matrix with biomarker, clinical operations, data management, regulatory and procurement colleagues, managing vendors, contracts and data transfer agreements while keeping studies audit-ready.

• Waltham, United States
• Hybrid
• US$123,000 – US$205,000 pa
• Lead

Owns operational delivery of diagnostics across early and late-stage oncology trials, from biosample collection and clinical trial assays at reference and central labs to audit-ready data. Works in a matrix with Diagnostic Strategy, Biomarker, Clinical Operations, Data Management, Regulatory, Quality and Procurement, plus external CROs, labs and vendors, and mentors colleagues as a subject matter expert.

CRO

• Reading
• Remote
• Lead
• Contract

Oversees end-to-end clinical data management for complex global trials, from study setup through database lock, acting as the primary client contact for data deliverables. Leads cross-functional teams, manages SAE/PK and external data reconciliation, timelines and budgets, and mentors junior staff. Fully remote with equipment provided, working across FSP delivery models.

Medidata Rave · Oracle InForm · MS Teams

• Reading
• Remote
• Mid-level
• Permanent

Oversees vendor activities across global clinical trials from study start-up through close-out, managing central lab, eCOA, IRT, ECG, imaging and patient recruitment vendors. Tracks vendor performance, KPIs and KQIs, drives site readiness and activation, and handles risk mapping, contingency planning and cost control. Home-based within Europe, working in a single-sponsor department.

eCOA · IRT · ECG +1

• London
• Remote
• Senior

Lead monitoring activities for assigned oncology clinical trial sites, from site activation through closeout, conducting both onsite and remote visits, source data verification and regulatory document oversight. Partner with a dedicated sponsor in an FSP model, driving enrollment, resolving protocol deviations and supporting audit readiness. Requires at least five years of oncology clinical research experience and up to 75% travel.

CTMS · EDC

• Maidenhead
• Senior

Leads safety surveillance and signal detection across a product's lifecycle, reviewing clinical and post-marketing data and contributing to aggregate safety reports and risk management plans. Partners with Global Safety Leads and cross-functional teams, mentors junior scientists, and supports regulatory responses.

Microsoft Excel

• London
• On-site
• Senior
• Permanent

Owns R&D extraction workflow development, adapting and optimising metagenomic DNA/RNA extraction methods across diverse, low-biomass and inhibitor-rich sample types, including HMW extractions for long-read sequencing. Designs controlled experiments, transfers validated methods to production and a global partner network, and works in a data-first lab environment feeding a large gene atlas.

DoE

• Oxford
• Hybrid
• Senior
• Permanent

Design and develop novel computational algorithms and AI/ML methods for translating metagenomic sequencing data into clinically actionable results, covering taxonomic classification and antimicrobial resistance. Validate and benchmark methods on public and internal datasets, then work with bioinformaticians and software engineers to embed them in scalable, reproducible workflows for an infectious disease diagnostic product.

Oracle Cloud · Long-Read Sequencing

• London
• On-site
• Senior
• Permanent

Lead research on the capabilities and risks of biological AI systems, designing evaluations, red-teaming studies and threat models, and developing safeguards across training, model behaviour and access. Work within the frontier model team with access to proprietary genomic data and biological expertise, shaping research priorities and publishing where appropriate.

EDEN · BaseData

• Burgess Hill
• Hybrid
• £49 – £86 ph
• Lead
• Contract

Leads authoring, review and lifecycle management of clinical and performance evaluation documentation for a global diagnostics organisation, including protocols, study reports, investigator brochures and regulatory submissions. Works cross-functionally with regulatory, quality, R&D and medical affairs teams, conducting literature reviews and synthesising complex clinical data under IVDR and GCP.

AI-enabled tools

• Field Force (England / Wales)
• Hybrid
• £32,690 – £60,710 pa

Site-facing role managing Phase I–IV clinical trial sites, acting as the primary contact between the sponsor and sites. Responsibilities include site initiation visits, training, on-site and remote monitoring, risk assessment and mitigation, and closeout activities, working closely with cross-functional teams to ensure data integrity and compliance.

• Leeds
• On-site
• Entry level
• Permanent

Prepare and handle investigational medicinal products in a cGMP clean room, applying sterile technique and GMP during live first-in-human studies. Work in pairs with Technical Officers on study set-up, dose calculations, batch records and equipment checks, with the clinic and pharmacy under one roof at an MHRA-accredited Phase I unit.

Outlook · Word · Excel +1

• London
• Hybrid
• Mid-level

Drives clinical supply forecasting and IMP budgeting for global trials, translating study protocols and recruitment projections into forecasting tools and monitoring deviations over 3-12 month horizons. Coordinates cross-functional IMP estimation and risk assessment meetings, aligning manufacturing, packaging and distribution to prevent stock-outs, while leading continuous improvement in a matrixed environment.

RTSM · Excel

• Leeds
• Hybrid
• Entry level
• Internship

A student placement supporting the Clinical Operations team in day-to-day coordination of clinical studies, including maintaining the Trial Master File (TMF/eTMF), tracking activities in CTMS, generating reports and distributing study supplies. Based in Leeds with flexibility to work remotely, though onsite working is preferred and may be required.

TMF · eTMF · CTMS +4