انتهت صلاحية هذا الإعلان الوظيفي

انتهت بتاريخ ١ أبريل ٢٠٢٦

CRA I, Ontario

Burlingtonدوام كاملعن بعد
Clinical ResearchICH-GCPSite MonitoringeCRFTravelPatient Safety Reporting

وصف الوظيفة

ICON plc is a world-leading healthcare intelligence and clinical research organization. As a Clinical Research Associate (CRA), you will conduct clinical trial site visits including evaluation, initiation, monitoring, and close out. You will oversee and report on the conduct of clinical trials at a site level and ensure excellence in operational and scientific delivery.

المسؤوليات

  • Conduct clinical trial site visits including evaluation, initiation, monitoring and close out
  • Oversee and report on the conduct of clinical trials at a site level
  • Identify opportunities and best practices with local/regional partners
  • Establishing and maintaining solid and professional relationships with site staff
  • Verification of electronic case report form data against written and electronic source documentation
  • Conducting IP accountability and reconciliation

المؤهلات

  • Bachelor's degree in a scientific or healthcare-related field
  • Minimum of 2 years of experience as a Clinical Research Associate
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
  • Fluent oral and written English language skills
  • Able and willing to travel up to 60% of the time
  • Possession of a full driver’s license

معلومات الوظيفة

تم النشر

٣١ يناير ٢٠٢٦

مستوى الخبرة

entry level

الحالة

منتهية الصلاحية