Senior Cra: Site Monitoring & Study Oversight

Iqvia Llc; Milano; On-site; EUR 40,000 - 60,000; Full time

Job summary

IQVIA LLC in Milano, Italy, is seeking a Clinical Research Associate to monitor sites and manage studies, ensuring protocol adherence and data quality.

You will conduct monitoring visits, coordinate with site staff, and support regulatory compliance across assigned sites in Italy, applying solid GCP/ICH knowledge and strong English communication.

This role offers collaboration with IQVIA's global teams and exposure to diverse therapeutic areas.

Qualifications

• Strong working knowledge of GCP/ICH guidelines.
• Minimum 3 years of on-site monitoring experience.
• Excellent communication skills in English, with the ability to coordinate across sites.

Responsibilities

• Conduct site monitoring visits and ensure protocol adherence and data integrity.
• Manage recruitment plans and coordinate with site staff.
• Ensure regulatory compliance and documentation quality across assigned sites in Italy.

Skills

GCP/ICH knowledge

English proficiency

Communication skills

Job description

IQVIA LLC is seeking a Clinical Research Associate responsible for site monitoring and study management to ensure protocol adherence, data quality, and regulatory compliance across assigned sites in Italy.
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You will conduct monitoring visits, manage recruitment plans, and coordinate with site staff, with IQVIA's global leadership in clinical research services.
The role requires xysqume solid GCP/ICH knowledge, 3+ years on-site monitoring experience, and strong communication skills in English; proficiency