Clinical Research Associate
Remote · Venice, Veneto, Italy
Job Summary
Clinical Research Associate to join TRIO’s Monitoring Resources team on a home-based role in Italy (Venice). Responsibilities include site visits (pre-study, initiation, monitoring, termination); ensuring adherence to FDA, ICH-GCP and local regulations; regulatory document completion and collection; data verification of source documents; ensuring FDA/ICH-GCP compliance; participating in budget negotiation; assisting with data validation and query resolution; mentoring junior team members. Requires oncology-trials monitoring experience, early-phase trial exposure, English fluency, a science-related Bachelor's degree, strong ICH-GCP knowledge, experience with clinical trial information systems, and up to 60% travel. TRIO offers competitive salary and benefits; AI tools may be used in candidate review. Prior to applying please review the Applicant Information Notice.
Required Qualifications
- 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
- Strong ICH-GCP knowledge
- Experience with clinical trial information systems
- Ability to travel up to 60% on average
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