Biotechnology Jobs

• Upper Providence
• Hybrid · 2 days in office
• US$340,500 – US$567,500 pa
• Director · manages people

Leads global development of a cancer vaccine asset from late-stage transition through approval and launch, acting as single point of accountability. Builds and leads a matrix Medicine Development Team spanning clinical development, immunology, manufacturing, regulatory, safety, medical affairs and commercial, and drives strategy, go/no-go decisions and lifecycle planning.

mRNA · Checkpoint Inhibitors

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$340,500 – US$567,500 pa
• Director · manages people

Leads global development of a cancer vaccine asset from late-stage transition through approval and launch, acting as single point of accountability. Builds and directs a matrix Medicine Development Team spanning clinical development, immunology, manufacturing, regulatory, safety, medical affairs and commercial, and drives strategy, go/no-go decisions and lifecycle planning.

mRNA · Checkpoint Inhibitors

• London
• Senior

Leads complex global and multi-regional clinical trials from start-up through close-out, with accountability for quality, timelines, budgets, regulatory compliance and sponsor objectives. Acts as primary strategic partner to sponsors and directs cross-functional teams across regions, with a focus on renal, obesity and MASH studies.

• London
• Lead

Lead the development of country, site and patient enrollment strategies for complex global clinical trials, analysing clinical and operational data to shape feasibility and study delivery. Present recommendations to clients and senior stakeholders, with a particular focus on APAC opportunities including China. Mentors colleagues and acts as subject-matter expert for planning tools.

• Harrow
• Remote
• Mid-level

Independently leads statistical aspects of low-to-moderate complexity clinical trials, developing complex analysis strategies and executing them with SAS or R. Reviews analysis datasets, quality-controls statistical deliverables, and contributes to trial design, analysis plans, and regulatory submissions. Works within global cross-functional teams, liaising with clients on data analysis, scope, and budget.

SAS · R

• Lisburn
• Senior · manages people

Senior Statistical Programmer supporting clinical trials within Parexel's FSP team, producing and QCing SDTM and ADaM datasets, tables, figures and listings using SAS. The role can act as Statistical Programming Lead, coordinating global teams, timelines and budgets while liaising with sponsors and Biostatistics and Data Management leads. It also involves mentoring staff and ensuring compliance with ICH-GCP and CDISC standards.

SAS

• Maidenhead
• Hybrid · 3 days in office
• Director

Leads strategic sourcing and evaluation of external innovation opportunities in Haematology, identifying preclinical to Phase 1 assets and shaping early partnering strategies. Sits on the Therapeutic Area Leadership Team, co-leads New Product Opportunity reviews, drives cross-functional due diligence and works with Business Development on deal execution. Hybrid, three days a week at an R&D hub site.

• Opfikon, Switzerland
• Hybrid · 3 days in office
• Director

Leads strategic sourcing and evaluation of external innovation opportunities in Haematology, identifying preclinical to Phase 1 assets and shaping early partnering strategies. Sits on the Therapeutic Area Leadership Team, co-leads New Product Opportunity reviews, drives cross-functional due diligence, and works with Business Development on deal execution. Hybrid, three days a week at an R&D hub site.

• London
• Hybrid
• £67,900 – £126,100 pa
• Senior

Co-leads cross-functional Clinical Trial Teams and global studies from planning through close-out, managing timelines, budgets, risks and inspection readiness. Partners across global and local functions on recruitment, data operations and vendor performance, while championing operational excellence and continuous improvement.

• London
• Hybrid
• £49,140 – £91,260 pa

Author and manage high-quality regulatory documents for clinical and submission teams, advising on writing standards and best practices. Collaborate cross-functionally on data analysis planning and presentation, lead writing plans and timelines, and apply AI tools to improve efficiency. Requires strong biostatistics understanding and pharmaceutical industry experience.

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…

• Newcastle upon Tyne
• £21,805 pa
• Entry level
• Contract

Investigates the molecular mechanisms of liver dysfunction in childhood POLG-related mitochondrial disease, focusing on Alpers-Huttenlocher syndrome. Uses quantitative untargeted proteomics and immunohistochemistry on donated post-mortem liver tissue, and generates hepatic organoids from patient-derived iPSCs for disease modelling and therapeutic screening. Based in the Newcastle Mitochondrial Research Group with a placement at the University of St Andrews.

iPSCs

• Cambridge
• On-site
• £20 – £24 ph
• Mid-level
• Temporary

Undertake routine and specialist microbiological and molecular investigations across bacteriology, Containment Level 3, serology, chlamydia and molecular diagnostics, interpreting and reporting results. Operate and maintain automated analysers, manage consumables and lab IT systems, and contribute to quality management, audits and SOP development. Based at Addenbrooke's Hospital within UKHSA's Public Health Microbiology team.

UKAS · HSE

• Newcastle upon Tyne
• £48,337 – £68,817 pa
• Senior
• Contract

Lead an independent research programme in transplant immunology, focusing on kidney transplantation injury and new therapies, while collaborating with nine senior investigators and the NIHR Blood and Transplant Research Unit. Contribute 0.2 WTE to undergraduate and postgraduate teaching and PhD supervision within the Translational and Clinical Research Institute.

Transplant Biobank

• Coventry
• On-site
• £36,320 – £46,970 pa
• Entry level
• Contract

Postdoctoral role in the Clostridial Cell Biology Group, leading molecular biology and experimental evolution work on vancomycin resistance in Clostridioides difficile. Collaborates with biochemists, bioinformaticians and clinical microbiologists across Warwick, Sheffield, Manchester and Leeds, and involves supervising PhD and masters students.