Research Assistant
Hamilton Health Sciences Hamilton region, Canada Posted 19 Sept 2026Full-time
About this role
• Identify eligible participants for various studies. • Recruitment of study subjects including informed consent process, randomization and implementation of study protocol procedures. • Maintain screening logs/records. • Completion of Case Report Forms (CRF’s). • Collection and transmission of source documents. • Review of Quality Control Reports and resolution of queries. • Schedule follow up with study participants as per study protocol. • Manage drug supply for study participants. • Arrange…
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