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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, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while guiding cross-functional teams and managing vendor performance. They also support redaction of confidential information and drive process improvements across disclosure operations.

CSL

United Kingdom

£31 – £35 pa Permanent

Genomics Assistant in Next Generation Sequencing Facility

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.

University of Cambridge

Cambridge, South East England, United Kingdom

On-site Permanent

Technical Program Coordinator, DDMR, London

Support AI-driven drug design programs by managing timelines, budgets, and stakeholder coordination. Facilitate cross-functional collaboration with internal teams and external partners like CROs. Help build and improve program management processes within a fast-paced, interdisciplinary environment focused on accelerating drug discovery through machine learning.

Isomorphic Labs

London, United Kingdom

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.

AstraZeneca

Macclesfield, United Kingdom

On-site Contract

SLDC Coordinator (Site Launch and Data Control) - 12-month / Secondment

This role involves managing the creation and modification of product packaging and master data within GSK’s supply chain, using systems like SAP, GLAMS, and CHAMPS. The coordinator ensures compliance with GMP and EHS standards while working cross-functionally to support new product introductions and pack changes. The position focuses on maintaining data integrity, meeting launch timelines, and driving process improvements in a regulated manufacturing environment.

GSK

Barnard Castle, 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.

NHS Professionals

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