Overview In this role, you will support multinational clinical studies by coordinating site activities and ensuring high-quality data. You will work within a cross-functional team to monitor sites, manage regulatory submissions, and help optimize recruitment. You'll contribute to compliant trial conduct aligned with GCP and ICH standards, impacting patient outcomes and study success. This is an international, growth-oriented opportunity with strong support for professional development and a stable, reputable employer.
Retribuzione / Benefits
career growth resources
flexible work schedules
therapeutic knowledge programs
company car
mobile phone
attractive benefits package
Responsabilità
Perform site selection, initiation, monitoring and close-out visits
Support development of a subject recruitment plan
Evaluate quality and integrity of site practices per GCP/ICH
Manage progress by tracking regulatory submissions, recruitment, CRF completion,



and data query resolutions
Collaborate with study site experts and client representatives
Requisiti fondamentali
University Bachelor's Degree and Master's Degree in scientific discipline or health care
CRA Certification as required by Ministerial Decree dated 15.11.2011
Experience in Pharma Industry and/or Clinical Trials
Very good computer skills including MS Office
Excellent command of English
Strong organizational, time management and problem-solving skills
Ability to establish and maintain effective working relationships with coworkers, managers, and clients
Flexibility to travel
Driver's license class B
communication
collaboration
problem-solving
MS Office
regulatory knowledge (GCP and ICH)
clinical trial monitoring

📌 CRA - MONITOR (Milano)
🏢 Iqvia
📍 Milano