IQVIA seeks an experienced Clinical Research Associate for a sponsor-dedicated role in Milan. The position involves conducting site visits, managing study progress, and ensuring regulatory compliance across clinical trial operations.
Responsibilities
Conduct site selection, initiation, monitoring, and close-out visits
Develop and support subject recruitment planning
Assess site compliance with GCP and ICH guidelines
Track regulatory submissions, enrollment, CRF completion, and data queries
Communicate with study site personnel and sponsor representatives
Requirements
Bachelor's and Master's degree in scientific or healthcare discipline
CRA Certification per Italian Ministerial Decree dated **********
Prior experience in pharmaceutical industry or clinical trials
Advanced proficiency with MS Office and computer systems
Fluent English language skills
Strong organizational and problem-solving abilities
Valid driver's license class B; willingness to travel
Compensation:
€32,****** - €53,****** base
📌 Clinical Research Associate, Sponsor Dedicated - Italy (Milano)
🏢 Iqvia
📍 Milano