Clinical Research Associate II

OverviewAs a CRA II at ICON, you contribute to designing and analyzing clinical trials, ensuring data quality and patient safety while supporting investigators and site staff. You’ll work cross-functionally to monitor trials, resolve data queries, and prepare key study documents. This role sits at the heart of advancing new medicines, offering...

Overview Join Allucent as a Start-Up Associate II to lead local site start-up activities for clinical trials. You will coordinate regulatory and ethics submissions and serve as the primary point of contact with authorities, investigators, and sites through the initial study phase. You will manage documentation, timelines, and country-specific requirements...

OverviewIn this role you support multicenter clinical studies by monitoring sites to ensure protocol adherence and data reporting per GCP/ICH guidelines. You will drive site communication, training, and recruitment alignment to project needs, and manage study progress and documentation in collaboration with the study team. The role includes ensuring TMF/ISF...

OverviewIn this CRA role at Medpace you will support the integrity of clinical studies across pharmaceutical and medical device development. You'll join a training-focused program (PACE) that accelerates your skills toward independent CRA responsibilities. You work across sites, regulators, and cross-functional teams to ensure compliant trials and data...

OverviewIn this role you join Medpace's Clinical Monitoring team in Italy to perform site monitoring, qualification, initiation, and closeout visits while ensuring protocol and regulatory compliance. You will verify investigator qualifications, manage data integrity, and support site performance to drive successful clinical trials. Travel up to 60-80%...

OverviewIn 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...

OverviewIn this role you join Medpace's Clinical Monitoring team in Italy to perform site-based monitoring activities for clinical studies. You will receive comprehensive training and work either remotely or from an office, contributing to study integrity and regulatory compliance. You collaborate with site staff and cross-functional teams to ensure quality...

OverviewAs Project Manager at Alira Health, you will drive the efficient execution of study protocols within scope, budget, and regulatory guidelines. You will partner with the Clinical team, sponsors, and vendors to keep trials on track and deliver timely status updates. You'll lead cross-functional study activities, oversee TMF processes, and support...

Overview In this role you will advance clinical studies by leading on-site and remote monitoring, ensuring data integrity and site partnership. You will drive study ownership across multiple sponsors and therapeutic areas, with a focus on deeper study knowledge and strong site relationships in Italy. You’ll mentor less experienced CRAs and operate in a...