Clinical Trial Associate

Questa posizione è in IQVIAIl processo di selezione sarà interamente gestito IQVIA.--The Trial Delivery Leader (TDL) serves as the single point of accountability for trial operational strategy, trial-level budget, quality, and on-time delivery of assigned clinical trials. This role represents the evolution of the Global Trial Leader (GTL), with a stronger...

Questa posizione è in IQVIAIl processo di selezione sarà interamente gestito IQVIA.--Global Trial Delivery Manager services provide for the global coordination of clinical trial management activities for internally managed and/or outsourced trials. These services lead the Study Management Team (SMT) and ensure global clinical operations deliverables...

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Start-Up Associate II (SUA II) to join our A-team (hybrid*/remote) in Italy! The SUA coordinates and performs local site start-up...

Clinical Trial Associate 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...

ICON Strategic Solutions is seeking a Clinical Trial Associate to support the design and analysis of clinical trials in a sponsor-dedicated model. You will assist with trial coordination, documentation, and cross-functional collaboration to drive timely and compliant study execution. The role requires a Bachelor's degree in a scientific or healthcare field,...

Overview In 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...

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...

L'IRCCS Ospedale San Raffaele, struttura clinica-scientifica-universitaria di rilievo internazionale e di alta specializzazione per diverse importanti patologie, sta ricercando uno Study Coordinator Junior da inserire all’interno del Clinical Trial Center – Area Trial StartUp.Attività principali: Il candidato si occuperà di seguire l’iter...

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...