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Jr Research Coordinator

Hamilton, ON
  • Number of positions available : 1

  • 31.94 to 40.95 $ 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
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

Requirements

Level of education

undetermined

Work experience (years)

undetermined

Written languages

undetermined

Spoken languages

undetermined