Wednesday, October 13, 2021 Reporting to the Team Leader, Ethics and Regulatory, the Ethics Research Associate will assist to conduct the ethics responsibilities of the Ethics and Regulatory (ER) office, within the Canadian Cancer Trials Group (CCTG). KEY RESPONSIBILITIES: • Reviews trial sample consent forms for necessary regulatory elements and appropriate lay language. • Reviews ethics documentation and consent forms for all centres being activated on CCTG trials. Review ethics reminders prior to their quarterly distribution to centres and addresses central office and centre concerns/queries regarding ethics reminders. • Corresponds with centres as necessary to request clarifications or additional information on Research Ethics Board (REB) documentation before activation. Communicates with centres regarding outstanding/inappropriate REB documentation in follow up to audit visits. • Maintains centre files by ensuring complete and current information is on file regarding REB documentation. Updates information in centres and ethics databases, as required. Find out more.
