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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.
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
This role involves performing routine environmental monitoring, water sampling, and microbiological testing (including sterility, bioburden, and endotoxin) for mRNA products in a GMP-regulated manufacturing environment. The analyst will support method transfers, data review, investigations, and compliance activities while working closely with internal teams and contract laboratories. Emphasis is placed on digital workflows, data integrity, and adherence to cGMP standards.
Oxford, United Kingdom
Lead translational data science initiatives using human genetics and multi-omic data to inform drug discovery decisions. Develop reproducible analysis workflows, integrate diverse biological and clinical datasets, and collaborate with cross-functional teams to identify drug targets and biomarkers. Mentor junior scientists and translate complex findings into actionable insights for project teams.
Stevenage, United Kingdom
Designs and leads the implementation of enterprise integration solutions using MuleSoft, focusing on secure, scalable APIs and data pipelines. Works closely with data and application teams to align technical architecture with business needs in a regulated biotech environment. Contributes to data strategy, including MDM and Data Lakehouse initiatives, while ensuring compliance with HIPAA, GDPR, and GxP.
Stevenage, United Kingdom
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