Your new company
You'll be joining a global biopharmaceutical organisation advancing novel therapeutics from research into the clinic. You’ll work in a highly collaborative, science‑driven environment supporting early clinical development and biomarker discovery projects across multiple disease areas.
The company is expanding their R&D teams and offers excellent development opportunities.

Your new role
This is initially a 12-month contract role that is very likely to extend for at least another year due to planned team expansion and increasing workload.
You'll be joining an experienced and diverse research group as a Senior Scientist / Principal Scientist specialising in transcriptomics.
You will support the delivery of clinical‑stage biomarker assays and provide expertise across transcriptomics and ideally high‑plex proteomics.
While this position requires in-depth knowledge of transcriptomic workflows this is not a bench based role - all experimental work is carried out by external CROs.

Key responsibilities include:

• Designing, planning, and carrying out transcriptomics and high‑plex proteomics experiments for non‑clinical and clinical studies
• Establishing fit‑for‑purpose assay workflows and generating high‑quality, reproducible data
• Acting as a subject‑matter expert in project teams and external interactions, including CROs
• Contributing to data analysis, interpretation, and clear communication of results
• Supporting project teams through scientific input at multidisciplinary meetings
• Managing workload and priorities to meet portfolio timelines
• Ensuring compliance with Health & Safety requirements and the Human Tissue Act (HTA)

What you'll need to succeed

• An MSc/PhD (or equivalent experience) in a relevant life‑science discipline, such as biology, biochemistry, or similar
• Hands‑on experience with transcriptomics workflows (eg RNA extraction, library prep, sequencing, etc), preferably for biomarker discovery/development
• Proven ability to deliver high‑quality data to project timelines
• Strong organisation, documentation, and communication skills
• Ability to work independently and adapt to changing priorities
• Knowledge of spatial omics or single‑cell RNA‑seq techniques would be an advantage, as would experience with qPCR/ddPCR validation, high‑plex proteomics, or bioinformatics analysis of omics data

Experience managing external partners/CROs would also be an advantage (or experience working within a CRO on similar studies).

ALL candidates must already hold the right to work in the UK without sponsorship until at least June 2027 (preferably June 2028 or beyond). No sponsorship is available for this role.

What you'll get in return
You'll get the chance to make a significant impact on the company's clinical assets, as well as work closely with a number of R&D teams and departments in a highly collaborative and friendly atmosphere.
The position also provides a generous daily rate and some work from home flexibility.

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.

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