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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

Director, Project Toxicologist – Immune Oncology (IO) Safety Science

Leads toxicology strategy for immune oncology drug development, integrating regulatory and preclinical safety science to guide candidate selection and regulatory submissions. Works across discovery and development to assess immune-related safety risks of novel immunotherapies. Provides scientific leadership, mentors junior toxicologists, and contributes to licensing decisions and external collaborations.

AstraZeneca

Cambridge, United Kingdom

Project Manager

Lead cross-functional projects within a regulated manufacturing environment, focusing on improving processes, delivering on time and on budget, and ensuring safety, quality, and compliance. Work closely with stakeholders across functions to drive operational excellence and support GSK's mission of delivering high-quality medicines and vaccines.

GSK

Barnard Castle, United Kingdom

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

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