IQVIA is seeking a CRA to monitor and manage clinical research sites in Italy, ensuring compliance with study protocols and regulations. The ideal candidate will hold a Master's degree in Life Sciences and have CRA certification. Responsibilities include conducting site monitoring visits, ensuring data integrity, and managing study documentation. Proficiency in Microsoft Office tools and strong communication skills are essential. This role requires effective time management and the ability to collaborate effectively with study team members.
J-18808-Ljbffr
📌 Clinical Trials Monitoring Specialist (Turbigo)
🏢 Altro
📍 Turbigo
Candidati a questo annuncio
Mostra le tue capacità professionali all'azienda, compila il form e lascia un tocco personale nella lettera di presentazione, aiuterà il recruiter nella scelta del candidato.