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Toxicologist (Non-Clinical pharmaceutical development) in Wiltshire


A pharmaceutical development non-clinical toxicology specialist with extensive experience in the specific requirements for the development and licensing of novel biological drug substances and drug products (primarily therapeutic antibody products) is required to provide expert toxicology advice to medical countermeasure project teams.

Provide strategic level toxicology advice to project teams to ensure that the development of biological products (primarily therapeutic antibody products) meet the GXP non-clinical and analytical requirements for the delivery of clinical trial approvals.


SC Clearance

Degree in relevant scientific subject

Significant non-clinical toxicology and analytical experience related to the development and licensing of biological products, specifically therapeutic antibodies through the MHRA.

Extensive experience of liaison with non-clinical test facilities, monitoring of studies and reviewing of contributing GXP reports and data.

A full and current understanding and practical experience of writing non-clinical summaries and sections for UK clinical trial authorisation applications (ie investigator brochures and IMPDs) and also of drafting non-clinical CTD modules and expert reports for Marketing Authorisation Applications (MAA).




Porton Down


Over £100,000
833 per day Max Ltd Company

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