Clinical Research Associate Jobs in Canada

Alimentiv is inviting qualified candidates to join a talent pool for Clinical Research Associate roles across multiple seniority levels. Candidates will be contacted for a qualifying call to discuss experience and timelines.

Clinical Operations team conducts global clinical trials to develop new therapies and improve patient outcomes. The Clinical Research Associate monitors sites, verifies data, ensures regulatory compliance, and supports investigators throughout the study lifecycle.

Clinical Research Associate (FSP) at Thermo Fisher Scientific in Toronto, Canada. Responsible for monitoring investigator sites, ensuring compliance with ICH-GCP, regulatory guidelines, and SOPs.

Clinical Research Associate on the IQVIA Clinical Trials team in Kirkland, Quebec. The role monitors study sites, conducts GCP‑compliant visits, manages recruitment plans, and ensures accurate data capture and regulatory submissions.

Clinical Research Team at a leading partner company drives drug development by executing global clinical trials. The Clinical Research Associate ensures trial sites operate safely and compliantly, performing monitoring, data verification, and regulatory support while coordinating with investigators and cross‑functional teams.

Clinical Research Associate (CRA) on IQVIA’s Clinical Operations team, driving high‑quality, compliant trials across Quebec sites. The role involves site monitoring visits, recruitment oversight, protocol training, and data quality reporting, ensuring regulatory alignment and patient focus.

Clinical Research Associate (CRA) on IQVIA’s Clinical Operations team, driving high‑quality, compliant trials across Quebec sites. Day‑to‑day duties include site monitoring visits, recruitment oversight, protocol training, and data query resolution.

Clinical Research Associate (CRA) on IQVIA’s Clinical Trials team, driving high‑quality, compliant studies across Quebec sites. Day‑to‑day duties include site monitoring visits, recruitment plan oversight, protocol training, data query resolution, and financial management.

Worldwide Clinical Trials is a global CRO seeking a Clinical Research Associate (Bilingual) – Oncology to support non-interventional studies across Canada. The role involves managing site research activities, from site identification and start‑up to data collection, safety reporting, and study close‑out.

Clinical Research Associate at AstraZeneca, responsible for delivering clinical study sites, ensuring compliance with ICH-GCP, managing site monitoring, data quality, and regulatory documentation. The role conducts remote and onsite monitoring visits, updates study systems, and collaborates with local study teams and investigators.

Clinical Research Associate at AstraZeneca Clinical Research, responsible for managing and monitoring clinical trial sites to ensure compliance with ICH-GCP and local regulations. The role conducts site initiation, monitoring visits (both remote and onsite), data verification, and collaborates with local study teams to drive study performance and quality.

Clinical Research team at Novotech ensures trial participants' rights and data integrity across global studies. The Clinical Research Associate builds site relationships, monitors compliance, and supports regulatory submissions while managing trial documentation.

Clinical Research Team at Jobgether advances global clinical development programs to improve patient outcomes. The Senior Clinical Research Associate serves as the primary liaison between trial sites and study operations, conducting onsite and remote monitoring, ensuring protocol adherence, data integrity, and regulatory compliance.

Clinical Operations team at Parexel drives oncology clinical trials across Canada. The Senior Clinical Research Associate oversees site selection, start‑up, monitoring, and closure, ensuring compliance with ICH‑GCP, local regulations, and risk‑based quality management.

Clinical Monitoring team at Altasciences oversees clinical trial oversight to ensure regulatory compliance and data integrity. The Lead Clinical Research Associate coordinates monitoring activities, mentors CRAs, develops monitoring plans, and drives metric collection across studies.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate, Bilingual, Oncology manages site activities from start-up to close-out, conducts initiation visits, ensures regulatory compliance, and supports data collection remotely.

The Clinical Research Associate II will oversee oncology clinical trials, ensuring sites follow protocols and regulations. Responsibilities include site visits, data monitoring, and regulatory compliance.

Senior Clinical Research Associate, Oncology – Francophone (Eastern Canada), IQVIA

Senior Clinical Research Associate in oncology, responsible for site monitoring, regulatory coordination, data review, and training across Canada and internationally.

Senior Clinical Research Associate in oncology, responsible for site monitoring, protocol review, data integrity, and regulatory compliance across Canada.