Parexel
A leading biopharmaceutical company in Augusta, Maine, is seeking a detail-oriented Regulatory CMC Project Manager. This role involves coordinating regulatory submissions, developing global regulatory tracking plans, and managing project meetings. The ideal candidate should have a Bachelor's degree in a relevant field and at least 3 years of experience in regulatory affairs, particularly in CMC. Strong project management and communication skills are essential, with an ability to manage complex projects in a dynamic environment. This position requires working East Coast hours, regardless of physical location.
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