Senior CRA for Multi-Sponsor Trials – Italy

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...

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...

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...

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...

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...

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...

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...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeWe are looking for a Clinical Research Associate I (CRA I) to join our clinical operations team in Italy.As a CRA I, you will perform and coordinate clinical monitoring and site management activities across investigator sites. Working through a combination of on-site and remote monitoring, you will...

If you are an experienced Senior CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you!Translational Research in Oncology (TRIO)is a global clinical research organizationdedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is...