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Global Regulatory Affairs Lead, Clinical Development

Remote • Posted 3 days ago
Onsite Full Time Consulting

Parexel is seeking a Regulatory Affairs Consultant/Senior Consultant to guide global clinical development programs through the regulatory landscape with strategy, insight, and collaboration. This highly visible role focuses on health authority engagement, submission planning, and lifecycle management across multiple regions.

You will lead regulatory strategies, coordinate cross‑functional teams, prepare meeting materials, and ensure compliance with FDA/EMA and ICH guidelines while advancing

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