Biotechnology Jobs

• Oxford
• On-site
• Lead · manages people
• Permanent

Build and oversee plant growth and phenotyping facilities, ensuring controlled, reproducible environments in growth chambers and greenhouses. Hands-on player-coach role covering planting, irrigation, pollination, sampling and harvest, plus pest and pathogen management, GMO compliance and phenotype data capture. Also shapes field trial operations and future team hiring.

Controlled Environment Growth Chambers · Greenhouses

• Oxford
• On-site
• Senior · manages people
• Permanent

Lead a flagship plant biotechnology research programme focused on photosynthesis, carbon assimilation and nitrogen fixation to boost crop yields and cut inputs. You will coach and oversee Group Leaders, run your own independent research, recruit scientists and postdocs, and drive stage-gated projects toward commercial and IP impact within a rapidly scaling institute.

• Durham, United States
• US$203,775 – US$339,625 pa
• Director

Leads the integrated real-world evidence and health outcomes strategy for mRNA influenza vaccines, designing and interpreting US post-marketing vaccine effectiveness studies across late-stage development, launch and post-marketing phases. Partners with clinical development, epidemiology, medical affairs, regulatory, biostatistics and market access teams, and builds collaborations with academic investigators, healthcare systems and data partners. Requires deep expertise in US vaccine effectiveness research, influenza epidemiology, real-world data and causal methods.

Medicare · EHR · Administrative Claims +1

• Waltham, United States
• On-site
• US$150,975 – US$251,625 pa
• Mid-level

Key member of the Clinical Development team contributing to the design, execution, analysis and reporting of clinical studies across all phases. Works cross-functionally with Medical Monitoring, Clinical Operations, Biostatistics, Data Management and Regulatory Affairs, reviewing safety, efficacy, biomarker and PK/PD data and supporting CSRs and regulatory submissions. Based on-site in Waltham, MA or London, UK.

• Reading
• Mid-level

Embedded with a global pharmaceutical sponsor, you act as the clinical supply representative in cross-functional study teams, owning supply strategy, vendor oversight and risk mitigation. Work spans protocol interpretation, label text, demand forecasting, packaging campaigns, IRT setup and temperature excursion management, with a strategic rather than operational focus.

IRT · RTSM · ERP +4

• London
• Freelance

Monitors Phase I-IV clinical trials across UK sites, conducting evaluation, initiation, interim and close-out visits in line with GCP and sponsor requirements. Works closely with the Clinical Trial Manager and Lead CRA, handling source verification, eCRF/EDC data review, query resolution and site training. Requires oncology monitoring experience and involves travel plus mentoring of less experienced CRAs.

EDC · eCRF

• Uxbridge
• Director

Serves as primary medical accountability for Phase 1–3 clinical trials in neuroscience, leading medical monitoring, safety assessment and benefit/risk analysis within a matrixed study delivery team. Partners with clinical scientists on protocol design, site interactions and health authority submissions, and builds relationships with principal investigators and thought leaders.

• Exeter
• £21,805 pa
• Entry level
• Contract

An interdisciplinary PhD studentship combining computational genomics at Exeter with stem-cell biology and CRISPR editing at Cambridge. The student will analyse whole-genome sequencing data from large multi-ancestry cohorts, integrate genetic signals with epigenetic maps and AI tools like AlphaGenome, and build iPSC-derived visceral and subcutaneous adipocyte models to functionally test prioritised regulatory variants.

AlphaGenome · DNANexus · Flow Cytometry +1

• London
• Hybrid
• Lead

Leads statistical work for post-marketing clinical trials, observational studies and real world data investigations, serving as Statistics lead on assigned projects. Develops protocols, analysis plans and TFL specifications, collaborating with clinical development, medical affairs, health economics and real world evidence teams. Requires strong SAS and R skills with a drug developer mindset.

SAS · R

• Leeds
• On-site
• Entry level
• Internship

A 12-month university placement within a global clinical data management team, supporting the full clinical trial lifecycle from project documentation and system set-up to data entry, validation, reconciliation and database lock. Interns work alongside experienced Clinical Data Managers on live trials, gaining hands-on exposure to clinical research technology and processes.

• Oxford
• Remote

Provide post-installation applications training and ongoing scientific support for customers using the Nanoimager microscopy platform. Troubleshoot workflow, sample and acquisition issues alongside Service and Product teams, drive adoption and contribute to renewals, and develop reusable training and knowledge-base materials. Involves 25% travel across the UK and Europe.

Nanoimager

• Norwich
• On-site
• £21,805 pa
• Entry level
• Contract

Investigates how G-quadruplex DNA and RNA structures regulate metabolic changes during fungal spore germination, using Aspergillus fumigatus as a model. The student will map G4 formation genome-wide, engineer mutants via CRISPR-Cas9, and apply NMR metabolomics and microscopy to study cell-wall remodelling and antifungal susceptibility within an interdisciplinary research environment.

CRISPR-Cas9 · NMR Spectroscopy

• Norwich
• On-site
• £21,805 pa
• Entry level
• Contract

Investigate why sexually antagonistic genes persist, using Drosophila to identify consistent loci and validate their sex-specific fitness effects via CRISPR-Cas9 allele swaps. Combines bioinformatics, genome engineering and sequencing, with training across evolutionary genetics, statistics and functional genomics at Norwich Research Park.

CRISPR-Cas9 · Long-read Sequencing · Single-cell Transcriptomics

• London
• £60,000 – £75,000 pa
• Senior · manages people

Lead the UK scientific affairs strategy for an international probiotic and functional food organisation, acting as senior scientific authority. Build KOL relationships across academia and healthcare, oversee human studies and research, ensure claims meet regulations, and manage a scientific affairs team while collaborating with European and global colleagues.

• Cambridge
• Director · manages people

Leads a team of medical writers and oversees strategic planning and drafting of complex regulatory submissions at the therapeutic area or portfolio level. Acts as subject matter expert, driving document strategy with cross-functional teams across Regulatory Affairs, Clinical Research and Clinical Data Science, plus process improvement and training initiatives.

Workday