Precision Medicine Group in Mexico is seeking a Senior Regulatory and Start Up Specialist to lead country-specific regulatory and site start-up activities for clinical trials.
You will manage CTAs, submissions to CA/EC, ICF reviews, essential document handling, and coordination with the Site Contracts team.
The role requires deep regulatory experience in Mexico, strong English communication, and the ability to mentor in-country staff while ensuring compliance with ICH-GCP and local regulations.
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📌 Senior Regulatory (Xico)
🏢 Precision For Medicine
📍 Xico
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