Clinical Research Associate

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Clinical Research Associate based in Canada.

This role offers the opportunity to contribute directly to the execution of global clinical trials that support the development of new therapies and improve patient outcomes. The Clinical Research Associate will operate at the intersection of science, regulation, and site management, ensuring clinical studies are conducted with the highest levels of quality, integrity, and compliance. Working closely with investigative sites and cross-functional clinical teams, the role spans the full study lifecycle—from site selection and initiation through monitoring, data verification, and close-out activities. It is a dynamic, field-based position requiring strong attention to detail, autonomy, and adaptability in a fast-paced research environment. The role also involves regular interaction with investigators and site staff, supporting protocol adherence and patient safety. This is a highly impactful position for professionals who thrive in clinical operations and want to shape the future of medicine.

• Conduct site qualification, initiation, monitoring, and close-out visits (on-site and remote), ensuring compliance with ICH-GCP Guidelines, applicable regulations, and study protocols.
• Verify informed consent processes, patient safety documentation, and adherence to ethical and regulatory requirements at investigator sites.
• Perform source data verification, review medical records, and ensure accuracy and completeness of clinical trial data entered into case report forms (CRFs).
• Manage investigational product accountability, including review of storage, dispensing, reconciliation, and compliance with protocol requirements.
• Maintain and reconcile essential trial documentation, including Investigator Site Files (ISF) and Trial Master Files (TMF).
• Document monitoring activities through trip reports, follow-up letters, and tracking systems, ensuring timely resolution of queries and issues.
• Support site engagement, recruitment, retention strategies, and participate in investigator meetings and clinical study trainings.

Requirements:

• Bachelor’s degree in life sciences, nursing, or a related field, or equivalent combination of education and clinical research experience.
• Strong understanding of ICH-GCP Guidelines and applicable regulatory frameworks.
• 1–3+ years of experience in clinical research, clinical monitoring, or a related clinical operations role (or equivalent exposure).
• Excellent attention to detail with strong analytical, documentation, and problem-solving skills.
• Ability to manage multiple site activities while maintaining high-quality standards in a fast-paced environment.
• Strong interpersonal and communication skills, with the ability to collaborate effectively with investigators and site staff.
• Willingness and ability to travel extensively (up to approximately 75%).

Benefits:

• Competitive compensation aligned with experience and market standards in Canada.
• Comprehensive health, wellness, and employee support programs.
• Flexible working arrangements depending on study and site requirements.
• Opportunities for continuous training in clinical operations, regulatory standards, and therapeutic areas.
• Career development pathways within global clinical research and project leadership functions.
• Exposure to large-scale international clinical trials and innovative therapeutic development programs.
• Supportive, collaborative environment with strong emphasis on learning and professional growth.