Requirements: English
Company: Translational Research in Oncology
Region: Rome , Lazio
If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today. TRIO is looking for a Clinical Research Associate to join our Monitoring Resources team. Reporting to the Monitoring Resources Coordinator, this position will be home-based in Italy. The main objective of the Monitoring Resources team is to effectively monitor TRIOs clinical trials according to contractual obligations and project deadlines, in compliance with sponsor protocols and SOPs. Responsibilities Conduct site visits, including pre-study, initiation, monitoring, and termination. Confirm adherence to all FDA, ICH-GCP, and local regulations. Ensure the completion and collection of regulatory documents. Perform data verification of source documents. Ensure implementation and compliance with FDA, ICH-GCP guidelines. Participate in budget negotiation and follow-up where applicable. Assist with data validation and query resolution. Mentor junior team members as required. Qualifications A minimum of 2 years of monitoring experience in oncology trials. An advanced level of oncology knowledge. Completion of a science-related Bachelors degree. Excellent knowledge of medical terminology and clinical monitoring processes. Strong knowledge of ICH-GCP guidelines. Experience with clinical trial information systems. Ability to travel up to 60% on average. What TRIO Can Offer You Competitive salary Paid time off Flexible working hours Core values: Integrity, Teamwork, Passion Position: Clinical Research Associate Roma, Italia#J-18808-Ljbffr