Clinical Research Associate - Canada

Clinical Research Associate in Canada performs site qualification, site initiation, interim monitoring, site management and close-out visits (on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Responsibilities include evaluating site/staff performance and providing recommendations, maintaining knowledge of ICH/GCP and SOPs, verifying informed consent, protecting subject confidentiality, assessing factors affecting subject safety and data integrity, conducting Source Document Review, verifying CRF data accuracy, applying query resolution remotely and on-site, using hardware/software to support data review, managing IP inventory and ISF/TMF reconciliation, training site personnel, supporting recruitment and retention strategies, tracking observations and action items, and collaborating with sponsor/Country staff. Qualifications require a Bachelor’s degree or RN, knowledge of GCP/ICH, and ability to travel up to 75% regularly. The posting notes this role may be for an upcoming opportunity rather than live posting; it emphasizes a global, collaborative clinical monitoring function within Syneos Health.”,