Biotechnology Jobs

• London
• Hybrid · 2 days in office
• US$284,625 – US$474,375 pa
• Director · manages people

Leads clinical development medical activities for cardiovascular and vascular programs across early and late-phase studies, shaping clinical development plans, study designs and translational strategies. Serves as clinical lead for a matrix team, providing medical monitoring, regulatory input and safety oversight while working with biology, regulatory, commercial and operations colleagues.

• London
• Hybrid · 2 days in office
• US$222,750 – US$371,250 pa
• Director

Provides clinical and scientific leadership across cardiovascular clinical development programmes, shaping study designs, translational plans and regulatory documents within the Respiratory, Immunology & Inflammation Research Unit. Leads a Clinical Matrix Team, oversees participant safety and medical monitoring, and works cross-functionally with biology, regulatory, statistics and commercial partners. Hybrid working with at least two days per week on-site.

• London
• Hybrid · 3 days in office
• Senior

Lead pharmacology and translational biology strategy for large molecule therapeutics, designing in vivo efficacy and complex in vitro functional assays. Act as Biology Lead on projects, coordinating internal workflows and external CROs, and collaborate with ML and computational biology teams to feed data into generative AI design loops.

AI · ML · Generative AI +1

• London
• Hybrid · 3 days in office
• Senior

Research engineers translate frontier research concepts into practical implementations, building and optimising state-of-the-art AI models such as Transformers, GNNs and diffusion models, plus the codebases, data pipelines and infrastructure for training and evaluation. The role sits in an interdisciplinary team of drug discovery experts and ML specialists, with a strong emphasis on experimentation, benchmarking and taking models from conception to production.

JAX · PyTorch · XLA +6

• 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

• 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

• 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

• London
• Remote
• Mid-level
• Permanent

Field-based medical affairs role acting as a scientific partner to healthcare professionals and thought leaders across the East Midlands, Yorkshire and East of England. Involves non-promotional scientific exchange, medical education, advisory boards, and supporting investigator-sponsored and real-world evidence studies within a neuroscience portfolio, working closely with UK, Ireland and global teams.

ABPI Code

• 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

• Oxford
• On-site
• Temporary

Serve as engineering owner for GMP manufacturing equipment at Moderna's Harwell facility, supporting the Norwood (MA) network. Provide hands-on floor support, troubleshoot complex mechanical and process issues, lead CAPAs and change controls, and drive continuous improvement and tech transfer for mRNA production. Requires close cross-functional work with equipment SMEs and end users.

TMIX · Single Use Mixers · Buffer Prep Vessels +4

• London
• £47,500 pa
• Entry level
• Contract

Lead an independent research project on eukaryotic cell cycle regulation in the fission yeast model, using cell biology, molecular genetics and biochemistry to study how CDK activity coordinates DNA replication, mitosis and division. The role sits in a collaborative lab and includes scope to develop new approaches and help support PhD students.

Schizosaccharomyces pombe

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

Develops and maintains Python and Java data pipelines that generate ChEMBL releases, plus other chemogenomics services like SureChEMBL, UniChem and ChEBI. Involves database administration, integrating external chemical databases, and collaborating with interdisciplinary scientists and engineers on curation and quality issues.

RDKit · Open Babel · InChI +7

• 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

• 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

• London
• On-site
• Entry level
• Internship

A 12-month industrial placement supporting in vivo pharmacology research within Pfizer's Internal Medicine Innovation Centre. Day-to-day work includes rodent husbandry and welfare, non-surgical procedures under a Home Office licence, ELISAs and in vitro potency assays for biologics, all under an experienced Research Director. Distinct for its strong focus on animal welfare and the 3Rs.

ELISA