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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.

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CureAge Therapeutics

London, ENG, United Kingdom

£212,000 – £251,000 pa Hybrid Permanent

Associate Director, Biostatistics

The Associate Director, Biostatistics, leads statistical contributions to clinical development programs, including study design, data analysis, and regulatory submissions. They collaborate with cross-functional teams, manage outsourcing, and ensure the quality and timeliness of deliverables.

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CSL

Global Safety Lead - Formulation Safety

Leads global safety strategy for formulation safety across the product lifecycle, focusing on clinical safety evaluation, signal detection, and risk management. Oversees production of key pharmacovigilance documents and ensures compliance with regulatory standards. Acts as safety representative in cross-functional teams and drives safety specifications and risk mitigation plans.

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CSL

£40,000 pa On-site Permanent

Scientist/Senior Scientist, Mass Spectrometry - Generative Biology Institute

This role involves developing and optimizing LC-MS workflows for single-cell proteomics and metabolomics, supporting researchers in experimental design and data interpretation, and collaborating with multidisciplinary teams to advance cutting-edge mass spectrometry techniques. The position is ideal for a scientist who enjoys method development, troubleshooting, and translating advanced MS technologies into high-impact research.

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Ellison Institute of Technology

Oxford, United Kingdom

£49,140 – £91,260 pa

Trial Vendor Senior Manager - Global Clinical Operations (GCO_

The Trial Vendor Senior Manager is a key member of the Clinical Trial Team, responsible for managing and overseeing clinical trial vendors to ensure study outcomes are met. This role involves direct operational oversight, vendor financial management, and collaboration with cross-functional teams to deliver high-quality clinical trials.

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Novartis

London, United Kingdom

On-site Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

Leads the design and execution of real-world evidence (RWE) and health outcomes studies to support oncology assets across their lifecycle. Focuses on generating robust, scientifically credible data to inform value propositions, market access, and reimbursement strategies. Collaborates with cross-functional teams and external experts to align evidence generation with payer, clinician, and regulatory requirements.

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GSK

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