RomaEUR 40.000 - 60.0003 giorni faIf you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! 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.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 requiredQualificationsA minimum of 2 years of monitoring experience in oncology trialsExperience in monitoring early-phase trialsCompletion 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 averagePaid annual leaveHealth insurance planSalary to be influenced (or determined) by education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market dataIf 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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