Clinical Research Associate needed to perform site monitoring and management for clinical trials in Italy. Responsible for conducting monitoring visits, managing recruitment, ensuring protocol compliance, and maintaining regulatory documentation in accordance with GCP guidelines.
Responsibilities
Conduct site monitoring visits including initiation, ongoing monitoring, and closeout
Develop and track subject recruitment plans with assigned sites
Administer protocol training and maintain regular communication with sites
Evaluate site compliance with protocol and regulatory requirements
Track study progress including regulatory submissions, enrollment, and data queries
Requirements
Bachelor's and Master's degree in scientific or healthcare discipline
Minimum 3 years of on-site clinical monitoring experience
CRA certification per Italian Ministerial Decree **********
Strong knowledge of GCP and ICH guidelines
Proficiency in Microsoft Office and standard computer systems
Fluent English, written and verbal communication skills
Organizational and problem-solving abilities
Compensation:
€33,900–€66,700 base annual salary

📌 Experienced Cra, Sponsor Dedicated - Italy (Lazio)
🏢 Iqvia
📍 Lazio