Regulatory Affairs Specialist - Global Submissions & Strategy
Curium Pharma
Curium is seeking a Regulatory Affairs Specialist to support US FDA submissions (NDAs/ANDAs/DMFs) and international drug applications. You will plan, author and manage eCTD filings for marketed products and coordinate with cross‑functional teams to ensure regulatory compliance. Responsibilities include assessing post‑approval changes, preparing labeling updates, maintaining regulatory databases, and mentoring entry‑level staff while staying current with evolving guidelines. #J-18808-Ljbffr Curium Pharma
Vacancy posted 1 day ago
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Maryland Heights, MO4 days ago
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