Principal Bioinformatician - Drug Development
| Posting date: | 27 February 2026 |
|---|---|
| Hours: | Full time |
| Closing date: | 29 March 2026 |
| Location: | London / hybrid, London, SL1 3WE |
| Remote working: | Hybrid - work remotely up to 3 days per week |
| Company: | Hays Specialist Recruitment |
| Job type: | Permanent |
| Job reference: | 4774924_1772187747 |
Summary
Your new company
Join a global biopharmaceutical organisation dedicated to transforming patient outcomes across multiple disease areas. You'll be part of a science‑driven environment that values innovation, collaboration, and meaningful impact and work with highly experienced colleagues.
Your new role
This is a permanent role within a well-established team where you will be reporting into senior bioinformatics leadership.The company has a collaborative and innovative atmosphere, where you will be supporting multiple projects within translational and clinical development across several therapy areas.
The role is hybrid, with c.3 days per week from home, though this can be negotiable for the right candidate.
As a Principal Bioinformatician within drug development, you will play a key role in generating biological insights from clinical stage omics data to support decision making across the therapeutic portfolio.
Major responsibilities will include:
- Processing, analysing, and interpreting multi‑omic (RNAseq, NGS, proteomic, etc) datasets from clinical studies
- Deriving mechanistic, biological, and treatment related insights from patient‑level data
- Developing and optimising analysis methods, pipelines, and computational workflows
- Ensuring reproducibility and best practice documentation for code and analyses
- Drafting high quality reports and contributing to scientific publications
- Applying SOTA (state‑of‑the‑art) tools for functional interpretation (e.g., pathway enrichment)
- Integrating omics outputs with clinical variables to enhance understanding of drug effects
- Operating autonomously while collaborating with cross‑functional scientific teams
What you'll need to succeed
A strong candidate will bring senior‑level experience in clinical bioinformatics along with:
- An MSc / PhD (or equivalent experience) in bioinformatics, computational biology, statistical genetics, biology, or a related subject
- Significant expertise in analysing bulk and single‑cell RNA‑seq from complex or clinical studies, with a significant preference for candidates who have done this in an industry (pharma, biotech, CRO) setting
- Experience with multi‑omics integration, functional interpretation, and pathway analytics
- Strong computational skills, including HPC, cloud platforms, and containerisation tools
- Proficiency in R and other commonly used bioinformatics programming languages
- Solid grounding in statistics, data mining, and biological data visualisation
- Ability to clearly communicate findings to both expert and non‑expert audiences
What you'll get in return
As well as an excellent opportunity to progress and develop your career within an innovative and collaborative work environment you'll be making a significant impact on the next generation of medicines and the patients they treat.
You'll also have plenty of flexible working options and a generous salary and benefits package.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.
Keywords: bioinformatics, bioinformatician, drug, discovery, pharmaceutical, biotech, clinical, principal, omics, RNAseq, single-cell, computational, analysis, pipeline, genetic, genomics, proteomics, epigenetic, spatial, data, integration, pathways, enrichment, causal, mechanisms, disease, biology, statistics, visualisation, programming, R, immunology, neuro, CNS, oncology, cancer, inflammation, respiratory