Jr. Research Coordinator
Ontario Province
Description
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.
Salary
31.01-39.76$ par heure
Characteristics
- Company
- Hamilton Health Sciences
- Experience
- Aucune
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