If you are an experienced Senior CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for youTranslational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting.

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Our passionate team is committed to providing cancer treatments of the future to the world of today.TRIO is looking for a Senior Clinical Research Associate to join our Monitoring Resources team.

Reporting to a CRA Line Manager, this position will be home-based in Italy.

This is a full-time position.ResponsibilitiesConducting 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. xlwpduy QualificationsA minimum of 2 years of monitoring experience in oncology trialsMinimum 5 years of previous CRA experienceExperience in monitoring early-phase trialsRead, write and speak fluent EnglishCompletion of a science-related Bachelor's degreeExcellent knowledge of medical terminology and clinical monitoring processStrong ICH-GCPs knowledgeExperience with clinical trial information systemsAbility to travel up to 60% on averageAbility to mentor and train new/junior CRAs on-site in a positive and effective mannerWhat TRIO Can Offer YouCompetitive salaryPaid annual leaveHealth insurance planFlexible working hoursLuggage allowanceMobile phone allowancePay Range: 55,000.00 to 65,000.00 Euro
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Senior Clinical Research Associate

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