Biotechnology Jobs

• Baar Onyx
• Hybrid · 2–3 days in office
• Director · manages people

Leads end-to-end clinical development of hematology oncology assets from first-in-human studies through registrational trials, regulatory approval and initial launch. Chairs governance forums, co-leads matrix asset teams and line-manages clinical development leads, medical directors and clinical scientists. Distinct for its portfolio-level scope across early- and late-phase programs and its cross-functional connector role spanning research, translational medicine and commercial strategy.

AI/ML

• Zug, Switzerland
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director

Serves as the physician within an oncology clinical program team, leading medical monitoring and safety oversight for genitourinary cancer studies. Interprets clinical and safety data, contributes to protocol development and regulatory interactions, and acts as a core member of the Clinical Matrix Team. Hybrid role requiring on-site presence at least two days per week.

AI

• Reading
• Mid-level

Conducts site monitoring visits including selection, initiation, monitoring and close-out, ensuring compliance with GCP and ICH guidelines. Manages site recruitment plans, protocol training, regulatory submissions and data query resolution, maintaining Trial Master File documentation. Focused on oncology studies within a biotech-focused clinical research team.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Reading
• Senior

Monitors oncology clinical trial sites through selection, initiation, monitoring and close-out visits, ensuring GCP and ICH compliance. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within a biotech-focused team supporting emerging biopharma sponsors.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Home Worker
• Remote
• £49,140 – £91,260 pa

Author and manage high-quality regulatory documents for medicines, working with cross-functional clinical and submission teams. Advise on regulatory writing standards, lead writing plans and timelines, and apply AI tools to improve quality and efficiency. Requires strong biostatistics understanding and global regulatory knowledge.

Artificial Intelligence

• Stevenage
• Hybrid
• Director · manages people

Accountable for onboarding and ongoing performance management of apheresis and treatment centres supporting clinical and commercial CAR T-cell therapies across the UK and Rest of World. Serves as the technical operations single point of contact, conducting site assessments, training centre staff, supporting quality systems and deviations, and managing process change rollouts. Involves up to 50% travel and possible management of contract employees.

Electronic Data Management Systems

• Oxford
• On-site
• £39,424 – £46,476 pa
• Mid-level
• Contract

Carry out research in spatial immunometabolism focused on the germinal centre reaction within the Clarke group at the Kennedy Institute of Rheumatology. The role involves developing new scientific techniques and experimental protocols, testing hypotheses, analysing data, contributing ideas for new projects, and providing guidance to postdocs, technicians and PhD students.

• 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

• 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

• London
• On-site
• Permanent

Runs a high-throughput sample processing pipeline, performing DNA extraction, normalisation and library preparation on soil, faecal and other environmental samples. Operates automated liquid handling platforms such as Myra9, logs everything in Benchling LIMS, and carries out QC checks while supporting R&D protocol testing in a CL2 lab.

Benchling · Myra9 · Hamilton +2

• 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

• Cambridge, United States
• Hybrid · 3 days in office
• Lead

Lead DMPK strategy across drug discovery projects, designing screening cascades and mechanistic experiments while integrating DMPK, PD and toxicology data for dose and safety predictions. Work closely with AI/ML platform teams to optimise computational ADME models and author regulatory sections, in a hybrid Cambridge, MA role.

Python · R

• 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
• £67,900 – £126,100 pa
• Senior

Lead the authoring of high-complexity regulatory documents and act as Program Writer for complex programmes, overseeing writing strategy, coordination, planning and resourcing. Partner with clinical trial and submission teams, shape data analysis planning, and champion AI tools to improve regulatory writing quality and efficiency.

Artificial Intelligence

• 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