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Hybrid Permanent

Director, Regional Ecosystem Lead (Northern Europe & UK)

This role involves leading CSL's presence in key innovation hubs across Northern Europe and the UK, building strategic relationships with biotech, academia, and investment networks. The Director will source and evaluate opportunities, lead deal teams, and represent CSL at industry events to enhance the company's reputation and deal flow.

CSL

United Kingdom

On-site Permanent

Associate Director, Safety Epidemiology – Global Patient Safety

Lead the design and execution of post-authorisation safety studies using real-world data to assess and communicate the safety profiles of AstraZeneca’s medicines. Provide strategic epidemiological input to regulatory submissions, safety signal evaluations, and diversity initiatives, collaborating with internal teams and external partners. Drive methodological excellence in pharmacoepidemiology and contribute to global patient safety decision-making across a broad product portfolio.

AstraZeneca

Chatham, ME4 4NP, United Kingdom

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

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