Biotechnology Jobs

• Oxford
• On-site
• Mid-level
• Contract

Design, roll out and maintain an ISO 9001-aligned Quality Management System across a research institute, covering document control, audit programmes and management reviews. The role also involves delivering QMS training and acting as a trusted advisor to programme leaders, on a 12-month fixed term contract.

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

Lead a flagship research programme in biological nitrogen fixation, engineering novel nitrogen-fixing systems into plants through metabolic and protein engineering. Recruit and manage a team of postdocs and PhD students, drive stage-gated translational research from lab to field, and build collaborations across EIT Oxford and commercial partners.

• USA - Pennsylvania - Upper Providence
• US$203,775 – US$339,625 pa
• Director

Provides scientific and strategic leadership for real-world evidence supporting GSK's mRNA vaccine portfolio, with a primary focus on influenza. Leads post-marketing vaccine effectiveness studies in the US, translating evidence needs into rigorous study designs and building 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

• USA - Pennsylvania - Upper Providence
• US$139,425 – US$232,375 pa
• Director

Acts as the operational hub for oncology assets, owning the integrated project plan, budget and risk inputs while driving critical-path acceleration and governance decisions. Partners with project leads to navigate uncertainty, facilitate high-performing teams and embed consistent project management practices across the pipeline.

Planisware · MS Project

• 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

• Reading
• Remote
• Mid-level
• Permanent

Oversees vendor activities across global clinical trials from study start-up through close-out, managing central lab, eCOA, IRT, ECG, imaging and patient recruitment vendors. Tracks vendor performance, KPIs and KQIs, drives site readiness and activation, and handles risk mapping, contingency planning and cost control. Home-based within Europe, working in a single-sponsor department.

eCOA · IRT · ECG +1

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

Investigates the repeated evolution of mimicry in Neotropical Corydoradinae catfishes using comparative and population genomics. The project analyses chromosome-level genomes, RNA-seq and whole-genome resequencing data to find signatures of divergent selection, selective sweeps and rapid pigmentation gene evolution, with training in bioinformatics, UNIX/Linux, HPC and R/Python.

RNA-seq · Whole-Genome Resequencing

• 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

• Norwich
• Hybrid · 3 days in office
• Mid-level
• Contract

You will own the delivery and reporting of two live Innovate UK projects, managing plans, milestones, budgets, risks and financial claims while coordinating consortium partners, funders and scientific teams. Working closely with the CEO, CBO and researchers, you will improve how projects are planned and tracked rather than inheriting a fixed system, and support future grant applications.

Innovate UK · UKRI

• Cambridge
• Director · manages people

Lead a biometrics team delivering statistical design, analysis and interpretation for oncology product development, from preclinical studies through regulatory submissions and health technology assessment. Represents statistical strategy at internal governance and external bodies such as health authorities and advisory boards, while mentoring statisticians and partnering with CROs.

SAS · R · Python

• High Wycombe
• Entry level
• Internship

A 12-month industry placement within the Integrated Data Analytics and Reporting function, focused on Clinical and Statistical Programming. The student applies SAS, R, Python, RPA and Power Automate to analyse trial data, build AI-driven tools and automate clinical reporting, while collaborating with programming experts across disease areas.

SAS · R · Python +4

• London
• Mid-level
• Permanent

Designs and implements generative models that learn intervention effects from single-cell perturbation and multiomic data, focusing on counterfactual prediction and experimental design. Works in interdisciplinary teams alongside experimental biologists to validate computational hypotheses and guide the highest-signal next experiments, with emphasis on causal coherence and real-world utility over benchmark fit.

• 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

• London
• Hybrid
• Entry level
• Permanent

Early-career scientist role in a Life Sciences team, generating therapeutic hypotheses by mining in-house genomic data with statistical methods to identify and triage drug targets. Also develops and optimises polygenic risk score tools for patient stratification, working with omic data using statistical and AI/ML approaches and communicating findings to internal and external stakeholders.

Git · GitHub · WDL +4