Clinical Research Associate (Italia)

Clinical Research Associate (Italia)

12 ago
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Icon Clinical
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Italia

12 ago

Icon Clinical

Italia

CRA II / Senior CRA ICON BiotechICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.We are currently seeking a Senior Clinical Research Associate (CRA) and CRA II's to join our diverse and dynamic ICON Biotech team. Per una comprensione completa di questa possibilità e dei requisiti per essere un candidato di successo, continui a leggere. As a CRA at ICON, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.Our biotech division of 8,000 people operates with a mindset aligned to small and mid-sized biopharma. Our tailored teams and management understand the different pressures that are faced by biotechs and will engage,



collaborate and share ownership in the delivery of your clinical trials.What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.Your Profile:Advanced degree in a relevant field such as life sciences, nursing, or medicine.Certification (Italian Law)Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.Prov

📌 Clinical Research Associate (Italia)
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