Regulatory Information Management Specialist

Merck

Merck & Co. seeks a Specialist in Information Management within Nonclinical Drug Safety to coordinate, assemble, and manage regulatory documents for internal studies and external efforts. The role supports PCD operations in Veeva and crafts internal processes to optimize document functions, collaborating with data scientists on AI-enabled drafting and review. You will contribute to report automation, control document lifecycles, and train end-users while aligning with regulatory expectations and #J-18808-Ljbffr Merck & Co.

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