Oncology Regulatory Submissions Lead – Europe (Hybrid)

A leading pharmaceutical company based in the UK is seeking a Senior Specialist for Regulatory Affairs within their Oncology team. The role involves providing administrative support for marketing authorization applications and managing regulatory submissions according to EU and UK standards. Candidates should have a relevant degree and several years of pharmaceutical industry experience. Strong organizational skills, attention to detail, and regulatory compliance knowledge are essential. This is a hybrid position with potential travel. #J-18808-Ljbffr