Clinical Research Coordinator

21 hours ago


Waterloo, Ontario, Canada ICON Strategic Solutions Full time
Job Title: Study Support Assistant

At ICON plc, we're committed to fostering an inclusive environment that drives innovation and excellence. We're seeking a highly motivated and detail-oriented Study Support Assistant to join our team.

Key Responsibilities:
  • Provide administrative support to the team, including tracking, filing, and coordinating tasks.
  • Assist Study Start Up Leads with submission documentation and guidelines.
  • Collate and verify submission documentation for regulatory authorities.
  • Coordinate submissions to CNEC and other relevant authorities.
  • Translate documents required for submission.
  • Update tracking systems and maintain departmental filing systems.
  • Coordinate payments to regulatory authorities and set up meetings.
  • Attend team meetings and generate meeting minutes.
Requirements:
  • University degree in Health Science or related field.
  • Two years of experience in Clinical Research or related industry.
  • Oncology experience required.
  • Strong understanding of Good Clinical Practices and International Committee on Harmonization principles.
  • Excellent social and interpersonal skills.
  • Ability to work independently and in a team environment.
  • Strong attention to detail and effective time management skills.
  • Good knowledge of MS Office and multiple computer systems.
About Us:

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to be a part of the ICON Strategic Solutions team, driving innovation and excellence in clinical development.



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