Advancing cancer research. Life-changing results.
Edmonton, Alberta
TRIO is a unique, full-service oncology clinical research organization (CRO) that leverages the strengths of our worldwide network of Investigators, academic leaders, patient advocates and our clinical research team to accelerate drug development. We’ve spent decades conducting oncology trials from inception to completion, focusing on the best research and science to guide the development of innovative and biologically sound therapies. This translational research model allows us to bring targeted concepts into clinics on the most rational development path. We find the shortest course to save lives. We are focused. We care. We deliver.
Remote · Canada
The CRA is responsible for conducting various site visits, including initiation and monitoring, while ensuring adherence to FDA and ICH-GCP regulations. Key duties include data verification of source documents, regulatory document collection, and assisting with query resolution.
Remote · Ottawa, Ontario, Canada
The Clinical Research Associate is responsible for conducting site visits, ensuring regulatory compliance, and performing data verification. They will also assist with budget negotiations, query resolution, and mentoring junior team members.
Remote · Canada
The CRA is responsible for conducting site visits, ensuring adherence to FDA and ICH-GCP regulations, and performing data verification of source documents. Additional duties include managing regulatory documents, assisting with query resolution, and mentoring junior team members.
Remote · Canada
The Clinical Research Associate is responsible for conducting site visits, including pre-study, initiation, monitoring, and termination. They must ensure compliance with FDA and ICH-GCP regulations while managing regulatory documentation and data verification.
