
Regulatory Affairs Associate: Submissions & Strategy
Katalyst CRO, Chicago, IL, United States
A leading clinical research organization in Chicago is seeking a detail-oriented Regulatory Associate to support the development and submission of regulatory documents. This role involves preparing regulatory documentation, coordinating with cross-functional teams, and ensuring compliance with regulations such as FDA and EMA. The ideal candidate will have a Bachelor’s degree and over 2 years of experience in regulatory affairs. This is a contract position offering opportunities in a dynamic environment.
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