Biotechnology Jobs

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

Lead in vitro and cellular pharmacology strategy for small-molecule drug design programs, defining screening cascades and guiding biophysical, biochemical and cell-based assays from hit identification to candidate selection. Bridge computational AI/ML predictions with laboratory validation, managing CRO partnerships and collaborating with chemistry, structural biology and translational teams.

SPR · ITC · CRO

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

Designs and implements translational strategies for small molecule oncology and immunology programs, from early discovery through candidate selection and clinical phase. Oversees CRO activities, PK/PD and safety assessments, and biomarker strategies, bridging computational predictions with laboratory validation. Some roles include managing 2-3 in vivo pharmacologists.

Machine Learning · AlphaFold

• London
• Director · manages people

Lead global labelling strategy for assigned products across early and late-stage development, lifecycle management and marketed portfolios, serving as Therapeutic Area Lead. Drive core labelling documents including CCDS, USPI and EU PI, lead health authority negotiations, and shape a future USPI operating model while championing digitalisation and AI-enabled labelling solutions.

FDA · EMA · ICH

• Manchester
• Senior

Monitors clinical trial sites across selection, initiation, monitoring and close-out visits in line with GCP, while driving subject recruitment and tracking regulatory submissions, CRF completion and data query resolution. Also trains site staff, maintains TMF/ISF documentation and may support site financial management and start-up activities.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• 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

• Oxford
• On-site
• £40,178 – £48,700 pa
• Entry level
• Contract

Conducts research characterising crosslinked proteins and lipids under a Wellcome Trust-funded grant, using proteome and lipidome methods including sample preparation, LCMS and data analysis. Manages project administration, guides junior researchers and students, and contributes to reports, publications and external seminars.

LC-MS · nanoLC-MS

• Oxford
• On-site
• £39,424 – £47,779 pa
• Entry level
• Contract

Develop novel statistical and machine learning methods for large-scale genomic, phenotypic and health data, covering areas such as genomic language models, multimodal and federated learning, and multi-ancestry methods. Implement reproducible research software, apply it to biobank-scale datasets, evaluate statistical and predictive performance, publish findings and guide junior researchers.

• Addlestone
• On-site
• £47,557 – £52,010 pa
• Senior · manages people
• Permanent

Lead a UKRI-funded Next Generation Veterinary Vaccines programme, investigating influenza, coronaviruses and zoonotic Disease X threats. Work across multidisciplinary teams using in vitro and in vivo approaches to design and optimise plug-and-play vaccine platforms, assessing immunogenicity, efficacy and antigenic variation. Includes line management, project coordination and work in SAPO4/ACDP3 containment facilities.

SAPO4 · ACDP3

• Oxford
• Hybrid
• Senior

Perform bioanalytical assays using molecular and cellular techniques such as ddPCR, qPCR, RT-qPCR and gel electrophoresis to quantify RNA in biological matrices. Support phase-appropriate assay development, qualification and validation within a GCLP-compliant clinical framework, partnering with internal and external labs and cross-functional teams. The role blends basic science research, bioanalysis and clinical development, with exposure to digital and automation tools.

Droplet Digital PCR · qPCR · RT-qPCR +2

• Harrow
• Remote
• Senior

Monitors clinical trial sites across the UK as the sole point of contact, conducting qualification, initiation, monitoring and termination visits and producing visit reports. Manages site quality, regulatory documentation and drug accountability while developing recruitment strategies to meet enrolment timelines. Fully decentralised role with less travel and a lower protocol load than industry peers.

Clinical Trial Management System · Electronic Document Management System · Excel +1

• Oxford
• Hybrid · 3–4 days in office
• Senior
• Permanent

Develops, validates and runs ligand-binding and cell-based bioanalytical assays generating pharmacodynamic and immunogenicity data for clinical mRNA programmes. Works in a GcLP-regulated lab using Thermo Watson LIMS and electronic notebooks, handling clinical samples, critical reagents, SOPs and validation reports while partnering with Clinical Operations and Sample Management.

Thermo Watson LIMS · Watson LIMS · LabVantage eLBN +1

• London
• Remote
• Senior

Responsible for the successful delivery of clinical studies at assigned investigator sites, acting as the primary point of contact for site management, monitoring, and study execution. Leads site preparation, initiation, routine monitoring, and close-out, conducting onsite and remote visits, source data review and verification, and CRF review while managing risk-based quality and regulatory compliance. Works within a local study team supporting a key sponsor, with travel across the UK and internationally.

CTMS · eTMF

• Addlestone
• £40,056 pa
• Mid-level
• Permanent

Design and execute scientific investigations into mammalian viral pathogenesis and host-pathogen interactions, ensuring work meets ISO9001, budget and customer requirements. Communicate findings via conferences and peer-reviewed journals, supervise staff and students, and pursue national and international research funding. Includes rostered on-call cover for weekend and Bank Holiday diagnostics.

ISO 9001

• Leeds
• On-site
• Senior

Lead early-phase clinical trials as Principal Investigator or Project Physician, taking studies from start-up through closeout and the Clinical Study Report. Work across first-in-human studies, multiple therapeutic areas and an NHS Trust collaboration, with on-call cover and mentoring of less experienced physicians.

MHRA · cGMP · NHS Trust

• Sheffield
• £32,722 – £37,369 pa
• Senior
• Contract

You will process samples for molecular and genomic analysis, maintain laboratory equipment, and support visiting researchers in a Genomics Laboratory. The role also involves training users new to molecular biology, advising external clients, and contributing to research and development that expands the facility's capabilities.

eDNA