Syneos - Clinical and Corporate - Prod is looking for a Regulatory Consultant CMC based in Belén de Escobar, Argentina. The role involves managing regulatory activities throughout the product lifecycle for small molecules. The ideal candidate will possess expertise in CMC and preferably Veeva Vault RIM, while also being available for collaboration in Eastern Standard Time.

Your responsibilities will include conducting research and managing regulatory submissions, as well as collaborating with multidisciplinary teams to ensure compliance and successful project delivery.