Clinical Research Associate

4 days ago

Athens, Attica, Greece Pharma Universe Full time

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.

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