Syneos - Clinical and Corporate - Prod is seeking a Regulatory Consultant CMC based in Zárate, Buenos Aires, Argentina. This role is responsible for managing regulatory activities through the product lifecycle and requires expertise in CMC and Veeva Vault RIM. The candidate must be available in Eastern Standard Time.

Key responsibilities include conducting regulatory research and ensuring compliance in regulatory submissions, collaborating with multidisciplinary teams, and effectively managing workflows to meet project deadlines.