Clinical Study Administrator — Hybrid eTMF

A leading global biopharmaceutical company in Milan seeks a Clinical Study Administrator to coordinate clinical study activities. Key responsibilities include maintaining trial documentation, supporting start-up activities, and collaborating with local study teams. The ideal candidate holds a Bachelor's degree and has proficiency in MS Office Suite, with at...

A global clinical research organization is seeking a Clinical Trial Manager to lead oncology-focused clinical studies in Italy. Key responsibilities include managing vendors, overseeing compliance with GCP, and coordinating study materials. The ideal candidate will have a bachelor's degree, a minimum of 5 years' experience in clinical studies, and strong...

Clinical Trial Manager – Italy | Advanced Clinical (FSP Model) Oncology focused Advanced Clinical is seeking an experienced Clinical Trial Manager to join our UK-based Functional Service Provider (FSP) team. This role will support global clinical studies and requires strong operational, vendor management, and monitoring oversight experience....

Are you ready to make a difference in the world of clinical trials? As a Clinical Study Administrator (CSA) within Country Operations Management (COM), you'll play a pivotal role in coordinating study activities from start-up to execution and close-out. Your mission is to ensure quality and consistency in trial deliverables, meeting time, cost, and quality...

Are you ready to make a difference in the world of clinical trials? As a Clinical Study Administrator (CSA) within Country Operations Management (COM), you'll play a pivotal role in coordinating study activities from start-up to execution and close-out. Your mission is to ensure quality and consistency in trial deliverables, meeting time, cost, and quality...

JOB SUMMARY Senior Clinical Consultant – Life Sciences (Rif. ANN ) We are CPL & Taylor by Synergos, an international digital‑solutions consulting firm specialising in the Life Sciences sector. Based in Italy, we support pharmaceutical and biotech companies across regulatory, pharmacovigilance, clinical trials, medical affairs and quality assurance. The...

Clinical Study Specialist (office based) ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. What you will be doing Organizes and delivers analyzable...

A leading clinical research organization in Milan seeks a Clinical Study Specialist to manage clinical trials by coordinating meetings, overseeing data evaluations, and ensuring regulatory compliance. The role requires a Bachelor's degree and at least 2 years of industry experience, with a focus on supporting global studies. Successful candidates will...

Clinical Monitoring Analyst (Cluepoints) - Remote Join to apply for the Clinical Monitoring Analyst (Cluepoints) - Remote role at IQVIA . This unique role within IQVIA is a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) and requires strong communication and organization skills. Experience with SAS programming is required. This role...

A leading clinical research organization in Milan is seeking a Clinical Trial Administrator. You will assist with clinical trial design and analysis, interpret medical data, and contribute to therapy advancements. Ideal candidates have a Bachelor's degree in a scientific field and strong organizational skills. The company promotes an inclusive environment...