Translational Research in Oncology (TRIO) is a global academic 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 Resource team. Reporting to the CRA Line Manager, this position will be a remote full-time freelance position based in Ireland. Responsibilities:Performing data verification of source documents;Conducting site visits, including pre-study, initiation, monitoring, and termination;Confirming adherence to all FDA, ICH-GCP, and local regulations;Ensuring implementation and compliance with FDA, and ICH-GCP guidelinesParticipating in budget negotiation and follow-up where applicableAssisting with data validation and query resolutionMentoring junior team members as requiredEnsuring the completion and collection of regulatory documentsQualifications:A minimum of 2 years of monitoring experience in oncology trialsExperience monitoring in early-phase trials will be valued. Completion 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 averageMust be legally authorized to work in the countryPrior to applying please review TRIO's Applicant Information NoticeTeamwork · Passion · Integrity · Innovation