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Jr. Research Coordinator

Hamilton, ON
  • Number of positions available : 1

  • 31.01 to 39.76 $ according to experience
  • Full time
  • Starting date : 1 position to fill as soon as possible

  • 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.

Requirements

Level of education

undetermined

Work experience (years)

undetermined

Written languages

undetermined

Spoken languages

undetermined