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Jr. Research Coordinator

1 month ago


Hamilton Ontario EH, Ontario, Canada Hamilton Health Sciences Full time
  • Identification and recruitment of study subjects including informed consent, randomization and implementation of study protocol (including follow-up visits with study participants)
  • Maintain screening logs/records.
  • Completion of Case Report Forms (CRFs).
  • Serious adverse event management and reporting
  • Manage all aspects of clinical trial start-up (contracts, ethics, in-hospital logistics, staff education)

Qualifications
  • Bachelor's degree in a relevant field of study.
  • Minimum 2 years previous experience in multi-center research studies/clinical trials.
  • Experience with the management of large clinical research studies and or databases.
  • Basic anatomy & physiology knowledge.
  • Working knowledge of ICH-GCP Guidelines and international research requirements.
  • Highly efficient computer skills, extensive experience with the Microsoft office suite.