Research Associate
Pubblicato il 12-09-2026 - Translational Research In Oncology in Italia
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 clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. TRIO is looking for a Clinical Research Associate to join our Monitoring Resources team. Reporting to a CRA Line Manager, this position will be home-based in Italy.
Conducting site visits, including pre-study, initiation, monitoring, and termination;
Confirming adherence to all FDA, ICH-GCP and local regulations;
Ensuring the completion and collection of regulatory documents;
Performing data verification of source documents;
Ensuring implementation and compliance with FDA, ICH-GCP guidelines;
Participating in budget negotiation and follow-up where applicable;
Assisting with data validation and query resolution;
A minimum of 2 years of monitoring experience in oncology trials;
Experience in monitoring early-phase trials;
Fluent in English;
Completion of a science-related Bachelor’s degree;
Excellent knowledge of medical terminology and clinical monitoring process;
Strong ICH-GCP knowledge;
Experience with clinical trial information systems;
What TRIO Can Offer You
Paid annual leave
Health insurance plan
Flexible working hours
Luggage allowance
Mobile phone allowance
Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.
If you are interested, please submit your resume in English. To support efficiency, TRIO may use limited AI tools during the candidate review process. To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI-generated responses during interviews or assessments. We want the opportunity to get to know you and your experience.