Global CMC Regulatory Consultant (Senior)

A global clinical research organization is seeking a CMC Regulatory Affairs Senior/Consultant to join their team in Des Moines, Iowa. The role involves contributing to regulatory strategy for both small molecules and biologics, preparing essential documentation, and collaborating with cross-functional teams to ensure compliance with global regulatory requirements. Ideal candidates bring 4-7 years of relevant experience, along with strong analytical and communication skills. Preference will be given to candidates in the Eastern Time Zone, but others will be considered. #J-18808-Ljbffr