Global Regulatory Start-Up Specialist II (CTR/CTIS)

Global Regulatory Start-Up Specialist II (CTR/CTIS)
Lisboa
Lisboa, Lisboa, Portugal

A global clinical research organization is seeking a Regulatory Affairs Study Start-Up Specialist II to manage regulatory submissions and provide support for clinical studies. The ideal candidate should have at least 3 years of experience in regulatory affairs within the CRO or pharmaceutical industries, and be fluent in English. This position offers opportunities for professional growth and is
- time based in Lisbon, Portugal.

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