Clinical Research Associate
Pubblicato il 03-10-2026 - Cti Clinical Trial And Consulting Services in Italia
Please submit your application in English
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What You'll Do:
Serve as main CTI contact for assigned study sites Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP Assist with or oversee study start-up activities, including feasibility, pre-study activities and site selection Collect, review and track essential/regulatory documents Participate in and complete all general and study specific training as required Participate in investigator, client and project team meetings; may include presentations Create and implement subject enrollment strategies for assigned study sites Ensure proper storage, dispensation and accountability of all Investigational Product (IP)
and trial-related materials Perform site management activities and provide ongoing updates of site status to Clinical Project Manager Conduct remote monitoring and complete related activities in accordance with study specific Monitoring Plan Utilize systems and reports to track subject status, subject case report form (CRF) retrieval / source document review (SDV), regulatory documents, and IP Assist with project-specific activities as member of Project Team What You'll Bring: 3 - 5 years clinical research experience as a CRA Life science background Excellent knowledge in ICH-GCP and regulatory requirement Fluent (at least Level B2) in spoken and written English About CTI Advance Your Career – We invest in your professional growth.
Our structured mentoring program, leadership development courses, and dedicated training department provide the support you need to excel. We also encourage ongoing education to help you achieve your professional goals. Join