Latest Gene Therapies Jobs

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Associate Director, R&D Project Management

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...

CSL
Hybrid Permanent
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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
Hybrid Permanent

Clinical Development Medical Director - Neuromuscular

Leads global clinical development programs in neuroscience, with a focus on neuromuscular or related disorders. Provides medical leadership across trial design, regulatory submissions, and safety monitoring, collaborating with cross-functional teams and external stakeholders. Plays a strategic role in advancing innovative therapies through clinical execution and scientific insight.

Novartis London, United Kingdom £83,510 – £155,090 pa
Hybrid Permanent

Clinical Development Medical Director - Neuromuscular

A Clinical Development Medical Director role focused on neuroscience, particularly neuromuscular conditions, with responsibility for shaping global clinical strategies and leading drug development programs. The position involves leading regulatory submissions, overseeing clinical trial execution, interpreting data, and engaging with regulatory authorities and key opinion leaders. Expertise in gene therapy and neurodegenerative disorders is highly valued within a collaborative, international environment.

Novartis £83,510 – £155,090 pa
Hybrid Permanent
Moderna logo

Principal Scientist, Bioanalytical & Molecular Assays

This role involves leading the development and validation of advanced molecular assays such as RT-qPCR, dPCR, and NGS to support clinical biomarker strategies across Moderna’s therapeutic pipeline. The scientist will work hands-on in assay design, optimization, and data interpretation, ensuring compliance with GCLP standards while integrating genomics, bioinformatics, and clinical insights. Collaboration with cross-functional teams is key to translating molecular data into actionable decisions for drug development.

Moderna Oxford, United Kingdom
Hybrid Permanent
Moderna logo

Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading scientific strategy and execution for immunogenicity and ligand binding assays in support of Moderna’s mRNA-LNP therapeutic programs. The Principal Scientist will oversee regulated bioanalytical activities including assay development, validation, and sample analysis, ensuring compliance with GcLP, GLP, and regulatory standards. The position emphasizes data integrity, cross-functional collaboration, and integration of emerging technologies, including AI-enabled data analysis, to accelerate clinical development.

Moderna Oxford, United Kingdom
Hybrid Permanent

Research Associate - Specialism in Bioinformatics with Potential Wetlab Experience

This role involves analysing high-throughput sequencing data to investigate RNA regulation in innate immunity, with responsibilities spanning computational analysis of multi-omics datasets and potential wet-lab experimentation. The researcher will apply bioinformatics techniques to study post-transcriptional regulation mediated by the ELAVL1 protein, using methods such as RNA-seq, eCLIP, and SLAM-seq. There is also an opportunity to contribute to experimental design, conduct CRISPR-based assays, and support training within a multidisciplinary team focused on inflammatory disease mechanisms.

University of Sheffield Sheffield, Northern England, United Kingdom £38 – £41 pa
Contract
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Global Safety Lead - Formulation Safety

Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...

CSL
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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