About this role
Clinical Research Associate Senior at MSD. Location: Brazil. Role: site management, monitoring, regulatory documentation Requirements: Manage clinical trial sites, ensure GCP/ICH compliance in oncology; fluent Portuguese and English; 65-75% travel; BA/BS in science preferred. Category: Research and Development (R&D) Seniority: Senior Level Tools: MS Office, CTMS, eTMF, Clinical IT tools, Regulatory systems Commitment: Full Time Workplace: Hybrid Languages: Portuguese, English