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Clinical Trials Coordinator

2 tygodni temu

Warszawa, Mazovia, Polska ICON Pełny etat
How You Will Succeed:

As a Clinical Research Coordinator, you'll be responsible for supporting Investigator Site staff in conducting clinical research studies according to project-specific requirements and regulatory guidelines. Your key responsibilities will include:

Monitoring Visits:
  • Support organization and execution of monitoring visits and audits at the Investigator Site.
  • Arrange visits, prepare documentation, and coordinate with relevant site personnel.

Data Management:
  • Enter patient-specific data into applicable clinical systems (eCRF, ASM, etc.).
  • Assist in resolving data queries and maintaining accurate records.

Patient Communication:
  • Arrange and coordinate patient visits and communication.
  • Collaborate with external service providers, such as central laboratories and couriers.

Reporting:
  • Prepare reports on completed activities as per established timelines.
  • Report any issues encountered during site operations to the Line Manager.