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Clinical Research Associate Pharma Universe(CRA II or above, Several sites across Italy). Responsibilities:. . Perform all types of monitoring visits (site selection, initiation, routine, and close-out) in line with ICH-GCP, protocol requirements, and SOPs . . Independently manage assigned study sites to ensure protocol compliance, patient safety, and data integrity . . Build strong relationships with investigators and site staff to support study progress . . Conduct source data verification and ensure timely and accurate data collection . . Maintain oversight of site performance and proactively address any issues . . Ensure proper handling and accountability of investigational product . . Contribute to site start-up activities, including document collection and regulatory submissions . . Participate in sponsor calls, team meetings, and ongoing training as required . . Requirements:. . Minimum of 1 year of independent monitoring experience is strictly required . . Strong knowledge of ICH-GCP and relevant local regulations . . Excellent organizational, communication, and problem-solving skills . . Ability to travel within Turkey . . Fluency in Italian and English . . Ideal for CRAs looking to gain further sponsor-side exposure within a supportive and professional environment.Company Location: Italy.