Clinical Research Associate

OverviewTranslational 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. 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.

ResponsibilitiesConducting site visits, including pre-study, initiation, monitoring, and terminationConfirming adherence to all FDA, ICH-GCP and local regulationsEnsuring the completion and collection of regulatory documentsPerforming data verification of source documentsEnsuring implementation and compliance with FDA, ICH-GCP guidelinesParticipating in budget negotiation and follow-up where applicableAssisting with data validation and query resolutionMentoring junior team members as required

QualificationsA minimum of 2 years of monitoring experience in oncology trialsExperience in monitoring early-phase trialsFluent in 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 average

What TRIO Can Offer YouCompetitive salaryPaid annual leaveHealth insurance planFlexible working hoursLuggage allowanceMobile 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.

Prior to applying please review TRIO's Applicant Information Notice.

To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI.

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