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Manages clinical trial case management activities, ensuring compliance with international and national regulations including GxP and pharmacovigilance standards. Oversees safety reporting, vendor performance, and case processing for serious adverse events, while acting as a key liaison for inspections and audits. Provides training, supports database enhancements, and ensures accurate coding and consistency in safety data analysis.
Performs bulk and single cell NGS protocols, spatial transcriptomics, and sample processing in a core facility. Operates Chromium X, Visium Cytassist, and Xenium platforms, with responsibilities including QC assessment, documentation, and customer liaison. Supports a research-intensive environment requiring precision, organisation, and technical adaptability.
Cambridge, South East England, United Kingdom
This role involves generating actionable commercial insights through competitive intelligence, market research, and forecasting to support Autolus' pipeline of T cell therapies. The associate will analyse market dynamics, monitor competitors, and synthesise data from multiple sources to inform strategic decision-making across commercial and clinical assets. It is a cross-functional position requiring coordination with external vendors and internal stakeholders to deliver evidence-based reports and dashboards.
London, W12 7RH, United Kingdom
Provides microbiological and environmental monitoring expertise to support aseptic manufacturing and clean room operations in compliance with cGMP standards. Oversees environmental control programs, conducts investigations, supports audits, and ensures regulatory compliance across production and QC facilities. Focuses on maintaining high standards in controlled environments and improving processes for patient safety.
Macclesfield, United Kingdom
This role involves designing and executing biological screening cascades to validate computational predictions in drug discovery. The scientist will lead biophysical, biochemical, and cellular assay development, collaborate with CROs, and bridge AI-driven insights with experimental validation across oncology and immunology programs. Close collaboration with medicinal chemistry, structural biology, and machine learning teams ensures data informs rational drug design.
England
Lead the technical development and implementation of a new labeling and secondary packaging operation at Moderna's Harwell site, ensuring compliance with GxP and safety standards. Establish maintenance strategies, lead capital projects, and drive continuous improvement using engineering excellence principles. Work closely with global teams and support digital integration in a high-growth biotech environment.
Oxford, United Kingdom
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