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Hybrid Permanent

Labelling Strategy and Development, Oncology Team Lead

Leads a global labelling team for oncology products, shaping clear, compliant, and patient-focused product labels. Interfaces with regulatory authorities and cross-functional stakeholders to drive labelling strategy and governance. Focuses on aligning regulatory, scientific, and commercial objectives across the oncology portfolio.

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GSK

Senior Clinical Trial Case Manager

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.

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CSL

On-site Contract

Specialist Quality - Environmental Assurance - 12 Month Secondment

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.

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AstraZeneca

Macclesfield, United Kingdom

£26 ph On-site Permanent Clearance Required

Band 6 Specialist Biomedical Scientist Haematology

As a Specialist Biomedical Scientist in Haematology and Blood Transfusion, you will work across central and satellite laboratories, processing and analysing patient samples, performing complex tests, and maintaining high standards of quality and safety. You will also support junior staff, manage stock, and participate in out-of-hours duties.

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NHS Professionals

Walton, Buckinghamshire, Buckinghamshire, HP21 7RY, United Kingdom

Hybrid Permanent

Senior Scientist (In vitro / Cellular Pharmacology), Cambridge, MA

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.

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Isomorphic Labs

England

Analyst, Quality Control, Microbiology

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.

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Moderna

Oxford, United Kingdom

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