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 · Alberta, Canada, British Columbia, Canada, Manitoba, Canada, Saskatchewan, Canada
The Clinical Research Associate is responsible for conducting site visits, ensuring compliance with FDA and ICH-GCP regulations, and performing data verification. They also assist with budget negotiations, data validation, and mentoring junior team members.
Remote · Alberta, Canada, British Columbia, Canada, Manitoba, Canada, Saskatchewan, Canada
The Clinical Research Associate will perform data verification, conduct site visits, and ensure compliance with FDA and ICH-GCP regulations. They will also assist with budget negotiations, data validation, and provide mentorship to junior team members.
Remote · Alberta, Canada, British Columbia, Canada, Manitoba, Canada, Saskatchewan, Canada
The Clinical Research Associate is responsible for conducting site visits, ensuring compliance with FDA and ICH-GCP regulations, and performing data verification. They will also assist with budget negotiations, data validation, and mentoring junior team members.
Remote · Alberta, Canada, British Columbia, Canada, Manitoba, Canada, Saskatchewan, Canada
The Clinical Research Associate will perform data verification, conduct site visits, and ensure compliance with FDA and ICH-GCP regulations. They will also assist with budget negotiations, data validation, and mentoring junior team members.
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 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.
