Biotechnology Jobs

• Stevenage
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director · manages people

Provides clinical and scientific leadership across translational and clinical studies within GSK's Respiratory, Immunology & Inflammation Research Unit, with a focus on aging. Leads a Clinical Matrix Team, designs clinical development plans and protocols, and oversees medical monitoring, safety and regulatory interactions. Hybrid working with at least two days per week on-site, initially in Stevenage before a planned relocation to Cambridge, UK.

• London
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director · manages people

Provides clinical and scientific leadership across early-phase clinical development programs in GSK's Respiratory, Immunology & Inflammation Research Unit, with a focus on aging research. Leads a Clinical Matrix Team, designs clinical development plans and study protocols, oversees medical monitoring and safety, and represents programs in regulatory interactions. Works cross-functionally with biology, translational sciences, commercial, regulatory and statistics partners.

• Reading
• Mid-level

Shapes and drives end-to-end clinical trial supply strategy, translating study protocols into kit designs, demand forecasts and packaging plans. Oversees vendors, IRT systems, distribution and temperature-excursion management while leading client and vendor meetings. Combines analytical planning with operational leadership across GxP-regulated clinical supply work.

Interactive Response Technology · Microsoft Word · Microsoft Excel +1

• Reading
• Mid-level

Embedded with a global pharmaceutical sponsor, you act as the clinical supply representative in cross-functional study teams, owning supply strategy, vendor oversight and risk mitigation. Work spans protocol interpretation, label text, demand forecasting, packaging campaigns, IRT setup and temperature excursion management, with a strategic rather than operational focus.

IRT · RTSM · ERP +4

• Cambridge, United States
• Hybrid · 3 days in office
• Senior · manages people

Lead computational drug design programs from hit identification through candidate selection, applying AI/ML to cheminformatics workflows and shaping the internal drug design engine. Roles span Program Lead or Computational Chemistry Lead, with some positions managing 2-3 computational chemists in a hybrid Cambridge, MA team.

REINVENT · AlphaFold

• London
• Hybrid · 3 days in office
• Lead

Lead formulation strategy for small molecules across drug discovery and preclinical development, designing technologies such as solid dispersions and co-crystals to improve solubility, stability and manufacturability. Work within an interdisciplinary team alongside AI/ML drug design platform groups, managing external CRO resources and authoring regulatory submissions.

ASAP

• 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

• London
• On-site
• Lead · manages people
• Permanent

Owns the end-to-end sample-to-sequence pipeline for the Trillion Gene Atlas, spanning DNA extraction, library prep and sequencing dispatch across Phase 1 and Phase 2. Bridges R&D and production by scaling validated protocols, applying Lean/Six Sigma to improve throughput, and leading a small lab team while monitoring data return with bioinformatics partners.

Illumina · Ultima · PacBio +3

• London
• On-site
• £27,500 – £30,000 pa
• Entry level
• Temporary

Processing blood and other biofluids from volunteer donors in a research services lab, including centrifugation, buffy coat and PBMC separation, reagent preparation and microbiological/viral testing of urine. Work follows Human Tissue Act, ISO 9001 and internal safety standards, with responsibility for maintaining laboratory records. Suited to someone starting out who has some blood or accredited lab experience.

• Oxford
• On-site
• Mid-level
• Contract

Designs and delivers immunogenicity and bioanalytical strategies for regulated clinical programmes, developing ADA, nAb, PK and PD assays using ELISA, MSD and cell culture. Works with multidisciplinary teams to validate assays, manage reagents and SOPs, and integrate digital and AI-enabled tools. Site-based at Harwell within a growing mRNA-focused team.

ELISA · MSD · LIMS +2

• Belfast
• £50,000 – £60,000 pa
• Lead · manages people

Leads a Clinical Method Development and Validation team, overseeing bioanalytical method delivery for a New Product Development programme. Provides technical leadership in a GLP-compliant lab, acting as expert in extraction techniques and optimising HPLC, UPLC and LCMSMS systems while mentoring the team.

HPLC · UPLC · LCMSMS +1

• Sheffield
• Remote
• Senior

Leads research design and analytical strategies for clinical trials, developing and reviewing statistical analysis plans and authoring reports, abstracts and manuscripts. Acts as functional lead on study teams, directing biostatistical activities, performing complex analyses in SAS or R, and quality-controlling deliverables while mentoring junior staff and liaising with clients on scope and budget.

SAS · R

• Guildford
• £48,337 – £70,878 pa
• Senior
• Permanent

Develop an independent, externally funded research programme as a Principal Investigator, applying AI and data science to human, animal and environmental health data within a One Health framework. Collaborate across medicine, veterinary science, computer science and engineering, secure UKRI/NIHR/Wellcome funding, publish high-impact work, and teach AI and data science at undergraduate and postgraduate level.

• Maidenhead
• Lead · manages people

Client-facing biostatistics role leading design and analysis of non-interventional and low-interventional studies using real-world data such as claims, EHR and registries. Applies causal inference methods, target trial emulation and synthetic control arms, authors SAPs and manages SAS programming teams, while supporting proposals, budgeting and bid defences.

SAS · CDISC

• 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