Clinical Research Associate II – Global Trial Monitoring

ICON Clinical Plc in Lombardia, Italy is seeking a CRA II to design and analyze clinical trials, monitor sites, collaborate with investigators, and contribute to study documentation. You will help uphold data integrity and patient safety while advancing innovative therapies.The role supports cross-functional teams in a fast-paced, global environment,...

OverviewCompetenze, Esperienza, Qualifiche: se possiede i requisiti giusti per questa opportunità, si candidi oggi stesso.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....

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...

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 & NutritionCandidarsi per questo ruolo è semplice. Scorra verso il basso e faccia clic su "Candidati" per essere preso/a in considerazione per questa...

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 **Possiede le qualifiche e le competenze giuste per questo lavoro? Lo scopra qui sotto e invii la sua candidatura per essere preso/a in considerazione.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...

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...

Quality Assurance (GCP) SpecialistCompany DescriptionPhidealive S.r.l. is an independent Italian full-service Contract Research Organization (CRO) operating as a Clinical Research Atelier.Unlike large global CROs, we work through a selective, highly tailored model, combining scientific expertise, regulatory rigor and close operational involvement in every...

ICON Clinical Plc in Lombardia, Italy is seeking a CRA II to design and analyze clinical trials, monitor sites, collaborate with investigators, and contribute to study documentation. You will help uphold data integrity and patient safety while advancing innovative therapies.The role supports cross-functional teams in a fast-paced, global environment,...