Global Regulatory Submissions Lead
Merida Biosciences
Merida Biosciences in Cambridge, MA is seeking an Associate Director of Regulatory Operations to lead global submission planning and lifecycle management across development programs. This hands-on role drives document readiness, eCTD publishing, cross-functional coordination with regulatory affairs, and strategic execution to ensure timely, compliant submissions while enabling efficient regulatory operations. #J-18808-Ljbffr Merida Biosciences
Vacancy posted 3 days ago
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