CMC Regulatory Project Manager & Writer
Katalyst CRO
Katalyst CRO is seeking an experienced CMC Writer/Project Manager to support regulatory submissions and deliver high-quality documentation for global health authorities. The role combines technical writing with project management to drive CMC deliverables across drug development programs. Responsibilities include authoring and reviewing CTD/eCTD sections, managing timelines, coordinating AR/DSUR docs, ensuring FDA/EMA/ICH alignment, and collaborating with cross-functional teams to mitigate #J-18808-Ljbffr Katalyst CRO
Vacancy posted 1 day ago
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