Research Coordinator I Risk Factor Modification - Toronto, Canada - Unity Health Toronto
Description
Duties & Responsibilities:
- Adhere to SOPs for clinical research
Qualifications
- Undergraduate Degree and 2 years of relevant experience, OR demonstrable equivalent combination of specialized education and experience
- Minimum 1 year IV experience, as strong IV skills required
- IV certified
- Previous experience running oral glucose tolerance tests is preferred
- Previous experience in research settings and clinical trials is preferred
- Preference for registered healthcare professional
- Training in TCPS2/GCP guidelines an asset
- Flexibility to adapt to changing workload
- Excellent interpersonal skills
- Professionalism and selfmotivation
- Good personal and program time/detail management skills
- Able to work independently and as part of a team
- Have proof of liability insurance
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