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Job description
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.
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Worksite address
cambridge, MA, 02140, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.