Clinical Research Associate

CRA II or above, Several sites across Türkiye)

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 :

Ideal for CRAs looking to gain further sponsor-side exposure within a supportive and professional environment.