Cancer Research UK (CRUK)

Compliance

• provide expert regulatory advice and support to cross-functional project teams
• supporting the preclinical development and clinical trials of a varied portfolio of novel oncology products
• managing the submission and on-going maintenance of optimal Clinical Trial Authorisation (CTA) applications
• leading internal discussions to respond to questions raised
• producing the Investigational Medicinal Product Dossier (IMPD) for designated projects

Regulatory Affairs Manager