Senior Clinical Research Associate – On-Site (Italy)

IQVIA; Milano; In loco; EUR 34.000 - 67.000; Tempo pieno

Descrizione del lavoro

IQVIA is seeking a Clinical Research Associate to perform site monitoring and ensure compliant data reporting per study protocol and regulations. The role involves monitoring visits, site training, and ongoing project communication across multiple sites in Italy.

The candidate should have a Master’s in a scientific field, 3+ years of on-site monitoring experience, and a CRA certification, with strong English communication and MS Office skills.

Competenze

• Bachelor's and Master's Degree in scientific discipline or health care.
• Requires at least 3 years of on-site monitoring experience.
• CRA Certification according to Ministerial Decree dated 15.11.2011.
• Good knowledge of GCP and ICH guidelines.
• Good written and verbal English communication.
• Proficiency in MS Office and mobile devices.

Mansioni

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) per contract scope and GCP.
• Collaborate with sites to drive subject recruitment to meet project needs.
• Administer protocol training to sites and maintain regular communication.
• Evaluate site practices for protocol adherence and regulatory compliance.
• Track regulatory submissions, recruitment, CRF completion and data queries.
• Maintain TMF/ISF documentation and visit reports.

Conoscenze

GCP/ICH knowledge

On-site monitoring

MS Word / Excel / PowerPoint

English communication

Time & financial management

Site coordination

Formazione

Bachelor's and Master's Degree in scientific discipline or health care

Strumenti

Microsoft Word

Excel

PowerPoint

Descrizione del lavoro

IQVIA is seeking a Clinical Research Associate to perform site monitoring and ensure compliant data reporting per study protocol and regulations. The role involves monitoring visits, site training, and ongoing project communication across multiple sites in Italy.

The candidate should have a Master’s in a scientific field, 3+ years of on-site monitoring experience, and a CRA certification, with strong English communication and MS Office skills.