Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable regulations
Manage assigned operational aspects for implementation of clinical trial activities from site activation through to database lock
Serve as the primary point of contact for assigned investigator sites during study conduct
Conduct onsite, remote monitoring for study site initiation, routine monitoring and study site closure activities
Monitor site level adverse events and collaborate with the Drug Safety Unit
Submit all required reports and documentation within required timeframes
Identify and resolve investigator site issues and develop corrective actions

Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience
Must be fluent in English
Significant travel across whole Turkey
Valid driver’s license and passport required

Senior Clinical Research Associate I – FSP

Key skills