IQVIA is seeking a CRA to monitor and manage clinical research sites in Italy, ensuring compliance with study protocols and regulations.
Faccia ora il prossimo passo nella sua carriera: scorra verso il basso per leggere la descrizione completa del ruolo e invii la sua candidatura.
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.
xysqume
This role requires effective time management and the ability to collaborate effectively with study team members.
#J-*****-Ljbffr
📌 Clinical Trials Monitoring Specialist (Bardi)
🏢 Iqvia
📍 Bardi