Global Regulatory Strategy Lead for Clinical Trials
Parexel
Parexel is seeking a Regulatory Affairs Consultant/Senior Consultant to guide complex global clinical development programs through the regulatory landscape with strategy, insight, and collaboration. This role focuses on health authority interactions, submission planning, compliance oversight, and strategic input across major markets. The ideal candidate has 5+ years in Regulatory Affairs with experience in FDA/EMA requirements, IND/CTAs, and cross‑functional leadership. #J-18808-Ljbffr Parexel
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