Senior CMC Dossier Lead: Regulatory Submissions
BioSpace
AbbVie seeks a Program Manager, CMC Dossier Management to develop and oversee CMC regulatory deliverables, including INDs/IMPDs and Marketing Applications. You will coordinate content plans, source document maps, rosters, and timelines using standardized PM tools to ensure on-time submissions. Responsibilities include monitoring submission progress, maintaining rosters, supporting cross-functional teams with risk analysis, and driving process improvements.
#J-18808-LjbffrVacancy posted 1 day ago
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