Clinical Research Associate Jobs in Canada

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.

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.

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.

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.

Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to support clinical trial site management, monitoring, and close-out across Canada (British Columbia, Alberta, Quebec, Ontario) in a remote work model.

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.

Worldwide Clinical Trials is a global midsize CRO advancing treatments across Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. As a Senior Clinical Research Associate in Clinical Operations, you will manage site research activities across all study stages—from site identification and start-up (regulatory documents, contracts, budgets) to training, study maintenance, and close-out—while ensuring informed consent, safety reporting, and regulatory compliance.

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.

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 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.

IQVIA Biotech, a full-service CRO serving biotech sponsors, is hiring a Clinical Research Associate II (Attaché de recherche clinique II) for oncology monitoring. The CRA II monitors Phase I–IV clinical trials to ensure compliance with protocols, GCP/ICH, and regulatory requirements, managing site activities from start-up through close-out.

Perform site monitoring and management for multiple clinical trials in Montreal. Bilingual French/English required. Conduct selection, initiation, monitoring, and close‑out visits per GCP/ICH guidelines.

Senior Clinical Research Associate responsible for site monitoring, management, and regulatory compliance across multiple protocols. Must be bilingual French/English, based in Mississauga.

Full Service Outsourcing team at Covance conducts clinical trials in oncology and general medicine. The Clinical Research Associate monitors sites, ensures protocol compliance, manages data integrity, and handles SAE reporting while coordinating with vendors and study staff.

Experienced CRA II with oncology monitoring, fluent in French and English, responsible for Phase I‑IV trial oversight, site visits, training, data integrity, and regulatory documentation. Requires 1+ year onsite monitoring, 65‑70% travel, bachelor’s in life sciences or equivalent.

IQVIA Clinical Research Team builds and monitors clinical trials across therapeutic areas. The Senior ARC conducts site monitoring visits, manages recruitment plans, and ensures GCP/ICH compliance.

As Clinical Research Associate, you will make sure clinical trials at your assigned sites run to high standards of quality, compliance and patient safety. You will be a key link between Novo and investigators, monitoring progress, spotting risks early and helping sites deliver reliable data on time.

The Clinical Research Associate (CRA) at Ocugen supports the planning, start-up, execution, oversight, and closeout of assigned Phase 1–3 clinical studies. Day-to-day work includes coordinating site activities, serving as an operational contact for investigational sites, overseeing CRO and field CRA monitoring, maintaining CTMS/eTMF/EDC records, and supporting audit and regulatory-inspection readiness.

The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and the Sponsor's standards.