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Nova Scotia Health and IWK Health
Overview
The Research Assistant supports study management by facilitating REB submissions, developing source documents, and maintaining organized filing systems. They are also responsible for participant recruitment, data entry into electronic Case Report Forms, and coordinating communications between participants and research staff.
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Compensation
CA$24 - CA$31 / HOUR
Posted
7 days ago
ICON plc
The Informed Consent Writer is responsible for creating health-literate informed consent documents for clinical trials across various therapeutic areas. This includes collaborating with protocol authors and managing the design and planning of documentation to ensure timely delivery and regulatory compliance.
Salary not listed
21 days ago
