Clinical Research Associate

14 ore fa

WorkFromHome, Italia TRIO - Translational Research in Oncology A tempo pieno

Overview 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. Translational Research in Oncology (TRIO) is a global 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. Responsibilities 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; Mentoring junior team members as required. Qualifications 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-GCPs knowledge Experience with clinical trial information systems Ability to travel up to 60% on average What TRIO Can Offer You Competitive salary 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. We thank all candidates for their interest; only those selected for an interview will be contacted. #J-18808-Ljbffr

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