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Hybrid Permanent Part-time

Senior Computational Chemist, LNP Design

This role involves leading the computational design of lipid nanoparticles for nucleic acid delivery, using chemical and biophysical principles, AI tools, and molecular simulations. You will work closely with the experimental team to translate computational insights into testable strategies and refine formulations iteratively.

CureAge Therapeutics

London

US$212,000 – US$251,000 pa Hybrid Permanent

Associate Director, Biostatistics

Leads the full statistical contribution to a clinical development programme, defining statistical strategy and methodology for trial design, analysis and regulatory submissions. Represents Biostatistics in interactions with FDA, EMA and PMDA, manages CRO/FSP outsourcing, and provides thought partnership on innovative study design and Go-No Go criteria. Two positions available across multiple therapeutic areas.

CSL

Amsterdam, Netherlands

£45,000 – £50,000 pa On-site Permanent

Scientist I – Molecular Biology

Design and build large-scale synthetic gene loci and transgenic platforms for antibody discovery, using CRISPR/Cas9, RMCE and site-specific integrases. Hands-on molecular biology including PCR, NGS, plasmid construction and flow-cytometric immunophenotyping, within a small multidisciplinary team working from dry-lab design to wet-lab validation.

Alloy Therapeutics UK Ltd

Cambridge

£26,000 – £40,000 pa Hybrid Permanent

Biology - Technical Support Engineer

The Technical Support Engineer will provide on-site and remote support for NanoFCM's analytical devices, including installation, maintenance, and customer consultations. They will work closely with customers to ensure the proper use and troubleshooting of instruments, software, and reagents, while also maintaining detailed service documentation and coordinating with the sales team.

NanoFCM CO., LTD

Stevenage

Global Safety Lead - Formulation Safety

Provides medical and scientific expertise on clinical safety across the full product lifecycle, with emphasis on evaluating safety data during clinical development and post-approval. Chairs the Safety Management Team, oversees signal detection, aggregate reports (DSURs, PSURs, RMPs) and regulatory responses, and sets safety strategy for global cross-functional development and post-marketing teams.

CSL

Maidenhead

£65,000 – £80,000 pa Hybrid Permanent

Senior Regulatory Affairs & Quality Manager

This role involves leading the regulatory strategy for a cardiology medical device company, focusing on FDA, CE, and UKCA submissions, and ensuring compliance with international regulations. You will work closely with the senior team and regulatory bodies, driving the company's expansion into new markets.

Bluetree

Cambridge