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