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ICON plc
Overview
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.
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Compensation
Salary not listed
Posted
21 days ago
Probity Medical Research Inc
The Source Worksheet Development Assistant is responsible for preparing data capture tools and performing administrative tasks for clinical trials. They must ensure regulatory compliance and maintain accurate study documentation within the company's online platform.
CA$25 - CA$25 / HOUR
1 month ago
Centricity Research
The Clinical Screening Coordinator leads research-related recruitment initiatives and screens patients for clinical study participation based on protocol criteria. They are responsible for maintaining recruitment logs, managing databases, and performing clinical tasks such as obtaining vital signs and completing source documents.
CA$40,000 - CA$50,000 / YEAR
