Clinical Research Associate (Canada)
Core
Perform monitoring and site management to ensure clinical study sites conduct studies and report data according to protocol, regulations, and sponsor requirements.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data and regulatory compliance for life sciences and healthcare clients
Domain
Life sciences / Clinical research
Deliverable
physical/clinical work
Required skills
Site monitoring, subject recruitment management, protocol administration, regulatory compliance (GCP/ICH), data query resolution, TMF/ISF management, financial management
Preferred skills
CRA training program completion, prior monitoring experience, therapeutic knowledge
Technologies
Microsoft Word, Excel, PowerPoint, laptop, iPhone, iPad
Responsibilities
Conduct site monitoring visits (selection, initiation, monitoring, close-out), track subject recruitment plans, administer protocol training, evaluate site quality and integrity, manage study progress (submissions, enrollment, CRF completion), maintain Trial Master File and Investigator's Site File, generate visit reports and action plans, support site financial management
Seniority
Individual Contributor