Senior Clinical Research Associate | Hybrid Home/Office

Medpace; Italia; Hybride; EUR 43 000 - 76 000; Plein temps

Avantages offerts par ce poste

Training program

Travel opportunities

Résumé du poste

Medpace is seeking full-time Clinical Research Associates to join our Clinical Monitoring team in Italy. This home or office-based role supports site visits, data verification, and regulatory compliance across studies, with up to 60-80% travel nationally.

You will work with experienced investigators and cross-functional teams, receive comprehensive training, and contribute to safe, high-quality clinical development for biomedical therapies.

Qualifications

• Master degree in a health-related field required.
• CRA certification completed as per DMC 15/11/2011.
• Previous CRA experience is required.
• Willing to travel up to 60-80% nationally and speak English and Italian.

Responsabilités

• Conduct qualification, initiation, monitoring, and closeout visits at research sites per protocol.
• Communicate with site staff including coordinators and investigators.
• Verify investigator qualifications, training, facilities, and staff.
• Verify source documentation and data entry accuracy; ensure SOPs and GCP compliance.
• Ensure enrollment of eligible subjects and review regulatory documents.
• Monitor device/investigational product accountability and adverse events.
• Assess site recruitment and retention and propose improvements.
• Prepare monitoring reports and follow-up letters with findings and actions.

Connaissances

English

Italian

Communication

Formation

Master's degree in health-related field

CRA certification (per DMC 15/11/2011)

Outils

Microsoft Office

Description du poste

Medpace is seeking full-time Clinical Research Associates to join our Clinical Monitoring team in Italy. This home or office-based role supports site visits, data verification, and regulatory compliance across studies, with up to 60-80% travel nationally.

You will work with experienced investigators and cross-functional teams, receive comprehensive training, and contribute to safe, high-quality clinical development for biomedical therapies.