Clinical Research Associate II — Hybrid

Clinical Research Associate II / Senior Clinical Research (CRA) - ItalyJob Category: Clinical MonitoringRequisition Number: CLINI002065Posted : October 1, 2026Full-TimeRemoteLocationsShowing 1 locationItaly - RemoteDescriptionWhatYou'llDo:Serve as main CTI contact for assigned study sitesConduct site visits (pre-study [PSV], site initiation [SIV], interim...

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...

WhatYou'llDo: 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...

CTI is seeking a Clinical Research Associate (CRA) to serve as primary CTI contact for assigned study sites, conduct site visits (PSV, SIV, IMV, COV) and ensure monitoring deliverables meet ICH-GCP and regulatory requirements.You will support start-up activities, maintain essential regulatory documents, track subject status, and collaborate with project...

Medpace seeks full-time Clinical Research Associates for Italy, offering home or office-based work with substantial national travel (60–80%). The role supports the Clinical Monitoring team, performing site visits, data verification, and regulatory review to ensure protocol adherence and patient safety.Medpace provides comprehensive initial and ongoing...

Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr CRA II assures the implementation of project plans as assigned, functions as leader for projects...

ICON Strategic Solutions is seeking a Clinical Research Associate II to design and analyze clinical trials, ensuring data integrity and patient safety across sponsor-driven studies. You will monitor sites, review data, and contribute to study documentation, working with investigators and staff to maintain high-quality trial conduct.Ideal candidates have a...

Medpace is seeking full-time Clinical Research Associates to join our Clinical Monitoring team in Italy, with home or office-based work options. You will conduct qualification, initiation, monitoring and closeout visits, ensure protocol compliance, and support data integrity across multiple sites.Qualifications include a Master’s degree in a health-related...

CTI is seeking a Clinical Research Associate II / Senior CRA to support sites in Italy, focusing on regulatory compliance and timely deliverables. You will act as the main CTI contact for assigned sites and manage site visits throughout pre-study through close-out phases. The role requires 3–5 years of CRA experience with a strong life-science background,...