Experteer Overview As an experienced Clinical Research Associate, you will oversee site activities across the trial lifecycle to ensure regulatory compliance and data integrity. You will work with study sites and client representatives to meet recruitment and submission milestones, while maintaining high-quality practices in line with GCP and ICH guidelines. This role combines hands‐on site monitoring with cross‐functional coordination to drive trial success. Join a reputable, international environment that supports career growth and flexible work arrangements.
Retribuzione / Benefits Perform site selection, initiation, monitoring and close‐out visits
Support the development of a subject recruitment plan
Evaluate site practices for quality and regulatory compliance (GCP/ICH)
Manage progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolutions




Collaborate with study site experts and client representatives
Responsabilità Bachelor in scientific discipline or health care
CRA Certification as required by Ministerial Decree dated 15.11.2011
Experience in Pharma Industry 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
Requisiti fondamentali company car
mobile phone
attractive benefits package
career growth resources
flexible work schedules
J-18808-Ljbffr

📌 Clinical Research Associate, Sponsor Dedicated (Italia)
🏢 Altro
📍 Italia