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Jr Research Coordinator

Hamilton, ON
  • Nombre de poste(s) à combler : 1

  • 31.94 à 40.95 $ selon l'expérience
  • Temps plein
  • Date d'entrée en fonction : 1 poste à combler dès que 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
1. Bachelor Degree or higher in health related field or previous clinical trial experience in a similar capacity
2. Ability to work independently, excellent communication (both oral and written) and problem solving skills, and ability to
work flexible hours .
3. Proficiency in MS Access, Excel, Word, Powerpoint.
4. Previous experience in cardiovascular clinical trials an asset.
5. Experience with Framemaker and DataFax or similar data management software an asset

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