Experteer Overview In this role you will independently conduct site monitoring for clinical trials, collaborating with internal teams to ensure protocol compliance and support study recruitment. You will manage site visits, monitor data integrity, and address site-related issues while maintaining rigorous adherence to ICH GCP and regulatory standards. The position offers cross-site coordination, problem solving, and ongoing stakeholder communication to drive trial progress. This role provides an opportunity to contribute to high-quality clinical research within a collaborative, values-driven environment. Retribuzione / Benefits Qualification, initiation, interim, and close-out visits with proper documentation Prepare monitoring visit reports detailing site issues, resolutions,



and enrollment status Facilitate adverse event reporting and SAE reconciliation with source docs and CRFs Ensure CRF data integrity via thorough source data verification Investigational product accountability Regulatory binder review for required documents Collaborate with in-house CRAs and data management to resolve data queries Identify site issues and develop problem-solving strategies Maintain contact with study sites for protocol/GCP compliance and patient accrual assessment Audit preparation at study sites as needed Collaborate with CRAs to maintain team consistency Manage conflicting priorities to meet commitments Comply with ICH GCP, FDA regulations, and SOPs Participate in industry and client meetings Perform additional duties as assigned Responsabilità BS/BA from undergraduate program or equivalent experience 2 years of clinical research experience #J-18808-Ljbffr

📌 Clinical research associate (Italia)
🏢 Experteer Italy
📍 Italia