Biotechnology Jobs

• Oxford
• On-site
• Mid-level · manages people
• Permanent

Leads the end-to-end event delivery workflow for gene edited and transgenic crops, from transformation output through sampling, molecular confirmation, QC review and handover. Designs and validates genotyping assays (PCR, qPCR, ddPCR, KASP, NGS) and builds stage-gate criteria, LIMS-enabled tracking and vendor strategies across corn and wheat programmes.

Endpoint PCR · qPCR · ddPCR +6

• Oxford
• Hybrid
• Senior
• Permanent

Builds robust, scalable services such as APIs, CLI tools and software modules for scientific applications, integrating ML inference servers, hardware interfaces and data pipelines. Owns the full production path from architecture and coding to automated testing, benchmarking, deployment and observability, working within a multi-disciplinary team of data engineers, AI scientists and domain experts.

• London
• Hybrid · 2 days in office
• Director

Serves as the physician within oncology clinical program teams, leading medical monitoring, safety oversight and clinical data interpretation for genitourinary cancer studies. Partners with the Senior Scientist and cross-functional Clinical Matrix Team on protocol development, investigator engagement and regulatory interactions, with hybrid working of at least two days on-site per week.

AI

• Warsaw, Poland
• Hybrid · 2 days in office
• PLN 472,500 – PLN 787,500 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 working with at least two days per week on-site.

AI

• United Kingdom
• Remote
• Mid-level · manages people

Lead statistician role delivering analysis database creation, statistical analyses, and formatted tables and summaries with minimal oversight, while mentoring junior team members. Involves leading project teams, interacting directly with sponsors, developing statistical analysis plans and randomization schemes, and programming or validating statistical tables with a strong emphasis on efficacy endpoints using SAS.

SAS · SAS BASE · SAS STAT +2

• United Kingdom
• Remote
• Senior · manages people

Accountable for delivering clean clinical data on time and within contract for low-to-moderate complexity haematology/oncology trials, managing operational and quality aspects in line with ICH GCP. Develops monitoring plans, CRF documents and Trial Master File content, tracks timelines and metrics, and may handle start-up, ethics submissions and project financials. Works within a team of CTMs, with travel to sites and a focus on radiopharmaceuticals, cell & gene therapy and CAR-T studies.

Outlook · Excel · Word

• London
• Hybrid · 3 days in office
• Senior

Lead the hardening and scaling of an inference platform serving fleets of cutting-edge ML models for scientific applications. Set strategy and roadmaps, architect next-generation services to solve scaling limits, and partner with research, product and operations teams to align infrastructure with biotech R&D cycles.

Kubernetes · Google Cloud Platform · NVIDIA GPU +1

• Oxford
• On-site
• Entry level
• Temporary

Support assay development, qualification, validation and clinical sample testing within Moderna's Immunoassay group, generating bioanalytical data that informs clinical trials. Work is primarily lab-based (≥85% of time) under a study lead, with responsibility for data integrity, reagent preparation, equipment upkeep and compliance with GCP/ISO standards.

GraphPad Prism · LIMS · Word +2

• Bracknell
• Hybrid · 2–3 days in office
• £37 – £49 ph
• Senior
• Contract

Analyse large-scale single-cell, bulk transcriptomics and other omics datasets, and develop new computational methods to extract biological insight. Build scalable, well-tested software and workflows for atlas-scale data (millions of cells) and high-dimensional proteomics, acting as the analytical point of contact in multidisciplinary collaborations from analysis plan through to publication or portfolio decision.

Visium · Xenium · MERFISH +4

• Cardiff
• Entry level
• Permanent

Performing hair sample sectioning, preparing sample batches, and analysing laboratory samples for alcohol and drugs of abuse. Adhering to Standard Operating Procedures, completing documentation, and carrying out routine maintenance and calibration of laboratory equipment. Requires knowledge of ISO17025 and prior laboratory experience, with a degree in Biomedical Sciences, Biochemistry or a related discipline.

• Cambridge
• Director

Leads business process mapping, design and optimisation across CMC Regulatory Affairs, from development and registration through post-approval lifecycle management. Partners with IT, data owners and cross-functional teams to translate regulatory needs into digital, automation and AI use cases, then drives implementation, adoption and KPI measurement. Distinct for combining regulatory operations expertise with AI-enabled capability building in a global matrixed pharma environment.

Veeva Vault · Planisware · Signavio +2

• Cambridge
• Hybrid
• Senior

Hands-on bioanalytical role developing, optimising and running LC-MS/MS assays for small and large molecule DMPK studies in an early discovery setting, analysing matrices such as plasma, blood, brain, bile, faeces and urine. Combines complex mass spectrometry troubleshooting and method development with leading scientific projects, mentoring colleagues and driving novel assay innovation in a matrix team.

UPLC-MS · LC-MS/MS · Mass Spectrometry

• London
• Hybrid
• Director · manages people

Leads the development and execution of international regulatory strategy across European and Rest of World markets, from first-in-human through post-marketing. Represents Global Regulatory Affairs on core development teams, manages project plans and resources, and advises senior management. Also a people manager within the International GRA leadership team, driving process improvement and regulatory policy engagement.

EMA

• 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

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

Leads clinical development strategy for multiple myeloma cell therapy programs, overseeing trial design, conduct, reporting and regulatory submissions. Represents products in governance committees, provides medical monitoring, and manages a team of direct reports while building external thought-leader relationships.

Workday