Clinical Research Associate II – Global Trial Monitoring

As a CRA II at ICON, you design and analyze clinical trials, ensuring data integrity and patient safety while advancing innovative therapies. You will monitor sites, collaborate with investigators, and contribute to study documentation. This role supports cross-functional teams in a fast-paced, global environment and involves travel. You will help bring new...

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...

Evidilya, CRO digital-native del Gruppo SPRIM., che Progetta e conduce studi interventistici e Real-World Evidence su scala globale nei settori Pharma, Consumer Healthcare, Medical Devices e Food & NutritionÈ il candidato/la candidata ideale per questa opportunità? Lo scopra leggendo la panoramica del ruolo qui sotto.ricercaIn-House Clinical Research...

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...

** Please submit your application in English **Faccia ora il prossimo passo nella sua carriera: scorra verso il basso per leggere la descrizione completa del ruolo e invii la sua candidatura.What You'll Do:Serve as main CTI contact for assigned study sitesConduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out...

As Lead Trial Delivery Manager, you drive study-level execution and vendor oversight across countries, ensuring trial plans align with local capabilities. You will shape operational strategies, manage risk, and mentor team members to deliver high-quality clinical research. This role sits at the intersection of trial management and cross-functional delivery...

As Lead Trial Delivery Manager, you drive study-level execution and vendor oversight across countries, ensuring trial plans align with local capabilities. You will shape operational strategies, manage risk, and mentor team members to deliver high-quality clinical research. This role sits at the intersection of trial management and cross-functional delivery...

OverviewIn this role you support regional clinical study delivery to ensure trials run on time, within budget, and to quality standards. You collaborate with the Regional Clinical Study Manager, global teams, and site staff to coordinate feasibility, start-up, TMF, and site communications. You gain hands-on experience in clinical operations and regulatory...