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-LjbffrGlobal Regulatory Submissions Lead in cambridge at Unknown Company
This position is listed as full time and onsite.