Senior Regulatory and Start Up Specialist (Brazil)
PrecisionMedicineGroupJob Description
📋 Description Delivery of site activation readiness within assigned country/sites Prepare Clinical Trial Applications and submission dossiers for CA/EC Interact with CA/EC and handle responses Provide updates to Start Up Lead/Regulatory Lead and Project Team Maintain project plans, trackers, and regulatory tools Ensure compliance with local and international regulations 🎯 Requirements Bachelors’ degree in life sciences or RN or equivalent 3.5+ years as Regulatory or Site Start Up specialist English proficiency (professional level) Excellent communication and organizational skills Experience with computerized systems and MS Office Fluency in English and local language of country when applicable 🎁 Benefits Remote work options Equal Opportunity Employer Supportive regulatory team and cross-functional collaboration