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Associate Director, Clinical Trial Disclosure & Transparency

This role leads global clinical trial disclosure and transparency strategy, ensuring compliance with international regulations such as FDAAA 801, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while managing redaction of confidential information for public release. They act as a key liaison with regulatory bodies and internal teams, driving process efficiency and vendor performance across the clinical development lifecycle.

CSL

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.

Isomorphic Labs

England

On-site Permanent

QA Associate

The role involves supporting the quality assurance of autologous CAR T-cell therapies in a GMP-compliant environment, with responsibilities including batch record review, documentation control, label verification, and compliance risk identification. The position operates within a multi-product cell and gene therapy facility, contributing to batch release activities and inspection readiness across international markets. Work includes collaboration with internal teams and adherence to strict regulatory and safety standards.

Autolus

Stevenage, United Kingdom

Quality Governance & Partnership Senior Specialist

This role involves managing quality governance systems for raw materials and suppliers at GSK’s manufacturing site. The specialist ensures compliance with pharmaceutical regulations, oversees supplier quality workflows, handles change controls and audits, and maintains documentation for material specifications and supplier agreements. The position plays a key role in maintaining supply chain integrity and regulatory compliance within a highly regulated biopharma environment.

GSK

Barnard Castle, United Kingdom

Associate Process Leader (Trainee Manager) – Sterile Production

This role involves supporting sterile manufacturing operations within a cGMP environment, focusing on production planning, compliance, and continuous improvement. The candidate will gain experience in deviation management, root-cause analysis, and cross-functional collaboration with Quality, Engineering, and Operations teams. Emphasis is placed on developing leadership skills and contributing to a culture of safety, efficiency, and manufacturing excellence.

AstraZeneca

Macclesfield, United Kingdom

On-site Contract

(Fixed Term) Scientist, Immunogenicity, Bioanalytical and Molecular Assays

This role involves designing and executing bioanalytical and immunogenicity strategies to support mRNA-based therapeutic development. The scientist will lead assay development for clinical programmes using platforms like ELISA, MSD, and cell-based methods, ensuring regulatory compliance and robust data generation. The position emphasizes collaboration across multidisciplinary teams and integration of digital tools and AI to advance Moderna's pipeline.

Moderna

Oxford, United Kingdom