Regulatory Data & Authoring Analyst, Digital CMC

A global pharmaceutical company seeks a Senior Specialist in Regulatory Authoring to streamline and optimize regulatory documentation processes. The role involves mapping business workflows, collaborating with cross-functional teams, and enhancing data management practices. Ideal candidates should have a Bachelor’s degree in a relevant field and significant experience in regulatory submissions, with strong skills in project management and communication. The position offers a hybrid work model based in Delaware, with a competitive salary range of $114,700 to $180,500. #J-18808-Ljbffr