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Clinical Research Coordinator – Cardio‑Obstetrics Network

ubc

🇬🇧 English
Good Clinical Practice (GCP)

Description du poste

About the role

The University of British Columbia is establishing a pan‑Canadian Cardio‑Obstetrics network. The Clinical Research Coordinator will lead and support retrospective and prospective studies over the next five years, ensuring high‑quality clinical trial execution.

Key responsibilities

  • Assist in planning, organizing and delivering clinical trials in line with study protocols and Good Clinical Practice (GCP).
  • Prepare and submit ethics applications, manage renewals and amendments.
  • Develop tools such as source documents, checklists, case report forms and test worksheets.
  • Provide study information and education to participants, administer questionnaires, and coordinate subject visits with multiple departments.
  • Verify patient histories, obtain medical records, and communicate findings to physicians.
  • Enter and manage data in paper and electronic case report form systems.
  • Supervise research assistants, clerical staff and students, and report progress to investigators.

Required profile

  • Experience in clinical trial coordination or related research support.
  • Strong understanding of GCP and ethics submission processes.
  • Excellent organizational and communication skills.
  • Ability to work collaboratively with clinicians, nurses and research staff.

Required skills

  • Good Clinical Practice (GCP)
  • Case report form design and data entry

What we offer

  • Competitive monthly salary ranging from $4,567.04 to $5,385.67 CAD.
  • Opportunity to contribute to a national research network in cardiology and obstetrics.
  • Supportive academic environment with mentorship from senior investigators.

Questions fréquentes

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Source : ats:workday

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