Biotechnology Jobs

• Waltham, United States
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director

Serves as the physician within a clinical program team, leading medical monitoring and safety oversight for genitourinary oncology 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

• Stevenage
• Hybrid · 2 days in office
• Director

Serves as the physician within a clinical program team, leading medical monitoring and safety oversight for genitourinary oncology 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 with at least two days per week on-site.

AI

• Cambridge
• Lead · manages people

Lead scientific strategy for cardiac electrophysiology and translational ion channel research, acting as scientific lead across multiple integrated drug discovery programmes. Guide experimental design using automated patch clamp (Qube/Sophion), MEA systems and hIPSC-derived cardiomyocytes, while serving as primary client contact and mentoring scientists.

Qube · MEA Systems · Sophion

• Manchester
• On-site
• Entry level

Perform complex clinical procedures such as ECG, phlebotomy, spirometry, cannulation and cardiac telemetry on trial volunteers, and collect and report data per protocol. Support Phase I-IV studies at a hospital-based research facility, ensuring compliance with GCP and SOPs while orienting volunteers and assisting nursing colleagues.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• 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
• Hybrid · 3 days in office
• Lead

Drive DMPK strategy across drug discovery projects, designing screening cascades and mechanistic experiments while integrating AI/ML and PBPK modelling to predict human dosing, efficacy and safety windows. Work within an interdisciplinary team of drug design and machine learning specialists, authoring regulatory documents and optimising molecule design with chemistry leads.

R · Python · KNIME

• Home Worker
• Remote
• £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. Provide expert guidance to clinical trial and submission teams, shape data analysis planning, and champion best practices, new technologies and AI tools to improve writing quality and efficiency.

Artificial Intelligence

• Aylesbury
• £23 ph

Job summaryWe have an exciting opportunity for a Biomedical Scientist Microbiology at Buckinghamshire Healthcare NHS Trust to join the Microbiology Department at Stoke Mandeville Hospital. You will be responsible for performing specialist microbiology and serology investigations in accordance with departmental…

• Oxford
• On-site
• Entry level

Postdoctoral researchers join an interdisciplinary team fabricating three-dimensional living, synthetic and hybrid tissues for disease modelling, therapeutic testing and organ repair. Openings span cell biology, electrophysiology, bioinformatics, hydrogel science and tissue engineering, combining stem cell biology, bioprinting and device engineering within a group of about 15 members.

Multielectrode Arrays · Calcium Imaging · Optogenetics +4

• London
• Hybrid · 3 days in office
• Senior · manages people

Lead computational chemistry strategy across drug discovery programs, applying AI-first approaches to hit finding, molecular design and lead optimisation. Work with ML scientists to embed generative models into cheminformatics workflows, with some roles managing 2-3 computational chemists.

REINVENT · AlphaFold · Large Language Models

• United Kingdom
• Contract

Shape and drive strategic medical affairs initiatives in the Ophthalmology therapy area, working locally and globally within Roche UK's Medical Affairs Chapter. Involves data and insight generation, scientific partnerships, medical education, and mentoring peers while engaging the clinical community.

• London
• On-site
• Mid-level
• Permanent

Own the full post-training lifecycle for biological foundation models, from alignment strategy to production deployment. Design pipelines that adapt general-purpose models to therapeutic contexts, build validation frameworks linking model improvements to biological ground truth, and run experiments end-to-end on distributed GPU infrastructure. Collaborate with ML infrastructure and biology teams and contribute to open-source tooling.

OpenTargets · helical-package · GPU

• Maidenhead
• Hybrid · 3 days in office
• Director · manages people

Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare analyses and evaluations for regulatory compliance. Supports Safety Management Teams, conducts proactive safety data reviews, and serves as product point of contact, with hybrid working requiring three days on site.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Uxbridge
• Hybrid
• Director

As a member of cross-functional development teams, you will contribute to trial design, protocol development, analysis planning, and regulatory submissions, with the option to support a specific asset indication. The role involves authoring statistical analysis plans and clinical study reports, defending protocols at governance reviews, and providing statistical leadership on health authority requests. It requires 50% onsite presence in Uxbridge and proficiency in SAS, R, or Python.

SAS · R · Python