Clinical Research Associate Jobs in Canada

Parexel Clinical Research team drives global clinical trials to bring new therapies to patients. The Senior Clinical Research Associate manages site selection, start‑up, monitoring (both remote and onsite), data verification and regulatory compliance, collaborating with investigators and internal study teams.

Clinical Research Associate on the Clinical/QARA team at Profound Medical, advancing innovative MR‑guided thermal ablation therapies. The role drives end‑to‑end trial execution—site initiation, monitoring, data verification, and closeout—while ensuring GCP compliance and high‑quality TMF documentation.

A partner company seeks a Clinical Research Associate in Canada to manage clinical studies from start-up through closeout. The role involves monitoring Phase I-III sites, ensuring protocol adherence and data quality, while collaborating with investigators and cross-functional teams.

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.

PSI, a global clinical research organization dedicated to bringing new medicines to patients, seeks an experienced freelance Senior Clinical Research Associate. The role involves conducting onsite monitoring visits, performing source document verification, and managing site communications across Canada.

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 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.

Premier Research is hiring a Clinical Research Associate II (Eastern Canada) to join its Clinical Monitoring, Site Management and SSU team. The role supports biotech, medtech, and specialty pharma companies by performing on-site and remote monitoring for Phase I-IV clinical trials and device trials across oncology, pediatrics, and rare disease.

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 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.

Our partner company seeks a Senior Clinical Research Associate to support Phase II and III clinical studies across Canada. This remote role involves conducting on-site monitoring, ensuring data quality, and serving as the primary contact for clinical sites.

Traferox Technologies Clinical Research team drives innovative organ transplantation studies. The Clinical Research Associate supports trial start‑up, conduct and close‑out, manages documentation, tracks enrollment and ensures regulatory compliance.

Worldwide Clinical Trials is a global midsize CRO advancing clinical research across therapeutic areas including Oncology. As a Senior Clinical Research Associate in Ontario, you will manage research activities at clinical sites across all study stages—from site identification and start-up to maintenance and close-out—while ensuring regulatory compliance and patient safety.

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.

This Senior Clinical Research Associate role supports the company's mission to bring new medicines to patients by conducting onsite monitoring visits and ensuring study compliance. The position involves site communication, CRF review, and participation in audits within Canada.

AbbVie seeks a Clinical Research Associate II in Edmonton, Alberta to support its mission of delivering innovative medicines. The role involves monitoring clinical sites for Phase I-III studies, ensuring protocol adherence and regulatory compliance through qualification, initiation, and closeout visits.

PSI, a leading Contract Research Organization, seeks a Lead Clinical Research Associate to oversee clinical trial operations in Toronto. This role involves managing monitors, ensuring regulatory compliance, and coordinating site feasibility and startup activities across the region.

Clinical Research team at Parexel advances global health by managing clinical trials across therapeutic areas. The CRA conducts site visits, ensures protocol compliance, and safeguards patient welfare while building strong site relationships.

The Senior Clinical Research Associate II (Associé de recherche clinique II) at Pfizer manages, monitors, and closes out assigned clinical trial investigator sites across Canada to ensure patient safety and quality study execution in compliance with GCP, FDA, and Pfizer standards. Day-to-day duties include conducting onsite and remote monitoring, training site staff, resolving protocol and data issues, overseeing investigational product, and supporting enrollment and database release.

Join the global clinical research team supporting top pharmaceutical companies and biotechs to advance Alzheimer's disease innovation. As a Clinical Research Associate (Level II), you will conduct remote and on-site monitoring visits to ensure protocol compliance, data accuracy, and regulatory adherence across trials.