Senior Regulatory Affairs Lead (Contract) – FDA & CMC

Curium Pharma in St. Louis, MO, is seeking a Senior Regulatory Affairs Specialist. This role involves supporting US FDA applications and coordinating regulatory activities to ensure compliance with health authorities.

The ideal candidate should possess a Bachelor's degree in a scientific discipline and have over 5 years of regulatory experience. Strong attention to detail and excellent communication skills are essential. Opportunity to work in a dynamic environment.