Clinical Trial Associate

ICON is seeking a Clinical Site Associate in Milan to support site management activities and ensure trials are conducted efficiently and in compliance. You will contribute to operations, collaborate with CRAs, and help maintain trial documentation and systems.The role requires a life sciences background, experience in clinical research or regulated...

Clinical Trial Liaison - Italy ICON 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...

BeOne Medicines in Milano, Italy seeks an experienced Clinical Research Associate to monitor oncology trials across sites, ensuring adherence to ICH-GCP, local regs, and BeOne SOPs. You will perform feasibility and site identification, initiate and conduct visits, and support data quality and timely milestones.The role requires a BS in a scientific...

As Clinical Trial Administrator, you will keep clinical trials in Italy moving with accuracy and pace. Based in Rome, you will support the local study team from start-up to close-out – managing trial documentation, tracking progress, coordinating vendors and making sure investigator sites’ payments are on time. Your work keeps trials compliant and...

Are you being referred to one of our roles by a connection in Alira Health? Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be...

Overview As an Associate Clinical Trial Manager at Medpace, you join the Clinical Trial Management team to help oversee global trial activities and ensure timely, accurate execution. You will collaborate with project coordinators, clinical trial managers, sponsors, and sites, applying your analytical and academic background to clinical project...

Overview In this role you support and expand a network of clinical sites in Europe, focusing on feasibility, site selection, and study start-up. You will partner with cross-functional teams to optimize site performance and intelligence, driving efficient feasibility processes and strong site relationships. The role combines overseeing site relationships,...

Provide support to Clinical Affairs team to assure study site selection and conduct of the study by study sites in compliance with Good Clinical Practices, federal regulations, and Clinical Affairs SOPs through in-house and some on-site monitoring Conduct pre-study visits to assure the site has adequate facilities, staff, and subject population for...

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a...