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Clinical Research Associate

2 tygodni temu

Warszawa, Mazovia, Polska ICON plc Pełny etat

Clinical Research Associate (en)

ICON plc is a leading healthcare intelligence and clinical research organization that fosters an inclusive environment driving innovation and excellence.

The Clinical Research Associate role involves supporting Investigator Site staff in conducting clinical research studies according to project-specific requirements and regulatory guidelines.

  • Primary point of contact for Investigator Site Staff and Sponsor representatives
  • Supports organization and execution of monitoring visits and audits at the Investigator Site, including arranging visits, preparing documentation, and coordinating with relevant site personnel
  • Enters patient-specific data into applicable clinical systems and assists in resolving data queries
  • Arranges and coordinates patient visits and communication
  • Collaborates with external service providers, such as central laboratories and couriers
  • Maintains assigned sections of the Investigator Site File and patient documentation
  • Participates in internal meetings and teleconferences
What You Will Be Doing:
  1. Serve as a primary point of contact for Investigator Site Staff and Sponsor representatives
  2. Support organization and execution of monitoring visits and audits at the Investigator Site, including arranging visits, preparing documentation, and coordinating with relevant site personnel
  3. Enter patient-specific data into applicable clinical systems and assist in resolving data queries
  4. Arrange and coordinate patient visits and communication
  5. Collaborate with external service providers, such as central laboratories and couriers
  6. Maintain assigned sections of the Investigator Site File and patient documentation
  7. Participate in internal meetings and teleconferences
  8. Assist with additional study-related tasks as per the Investigator's requirements
  9. Report any issues encountered during site operations to the Line Manager
  10. Prepare reports on completed activities as per established timelines
  11. Perform a wide range of administrative tasks connected to the assigned studies, mainly working with eCRF, query resolution, ISF maintenance, being the first point of contact for the CRA, monitoring visit support, etc.
  12. Perform other duties as assigned by the direct Line Manager