Experienced Clinical Research Associate, Multi Sponsor

Medpace; Varese; In loco; EUR 42.000 - 56.000; Tempo pieno

Vantaggi offerti da questo lavoro

Flexible work environment

Competitive compensation and benefits

Competitive PTO packages

Structured career paths with growth

Company-sponsored employee events

Employee health and wellness

Descrizione del lavoro

Medpace is seeking an Experienced Clinical Research Associate (CRA) to join the Clinical Monitoring team in Italy. You will conduct site visits, verify investigator qualifications, and ensure protocol and regulatory compliance to support trials from initiation through closeout.

You will manage source data verification, data integrity, and timely reporting while traveling 60-80% nationally. Fluent in English and Italian, you will collaborate with site staff and cross-functional teams to drive

Competenze

• Master in health-related field.
• Previous experience as Clinical Research Associate (CRA).
• Willingness to travel 60-80% nationally.
• Fluent in English and Italian.

Mansioni

• Perform site monitoring visits and ensure protocol and regulatory compliance.
• Verify investigator qualifications, training, facilities, laboratories, equipment, and staff.
• Perform source data verification and apply good documentation practices (GCP/SOPs).
• Review regulatory documents and assess site recruitment and retention performance.

Conoscenze

Team collaboration

Communication skills

Presentation skills

Formazione

Master's in health-related field

Strumenti

Microsoft Office

Descrizione del lavoro

In this full-time role, you join Medpace’s Clinical Monitoring team to support site-based trials in Italy, helping advance clinical development for diverse therapies. You will perform monitoring visits, ensure protocol and regulatory compliance, and contribute to data integrity and site performance. The position offers comprehensive training and a clear path for professional growth within a global CRO. Your work will directly impact trial quality, patient safety, and timely study delivery.

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Conduct qualification, initiation, monitoring, and closeout visits per the approved protocol
• Coordinate with site staff including coordinators and physicians
• Verify investigator qualifications, training, facilities, laboratories, equipment, and staff
• Perform source data verification and ensure good documentation practices (GCP/SOPs) and report protocol deviations
• Confirm eligibility of enrolled subjects and perform regulatory document reviews
• Oversee medical device and/or investigational product/drug accountability and inventory
• Review adverse events and related data for accurate reporting
• Assess site recruitment and retention performance and suggest improvements
• Prepare monitoring reports and follow-up letters with actionable recommendations
• Master in health-related field
• Previous experience as CRA
• Willingness to travel 60-80% nationally
• Familiarity with Microsoft Office
• Fluent in English and Italian
• Strong communication and presentation skills would be considered a plus
• team collaboration
• Microsoft Office
• Good documentation practices (GCP)
• Regulatory document review

Experienced Clinical Research Associate, Multi Sponsor varese, lombardia, it