CRA II

This is a fully remote position, open to applicants in Canada.

📋 Description

• Execute site qualification, initiation, monitoring, and closeout tasks as assigned.

• Support clinical trial monitoring efforts and take ownership of deliverables.

• Ensure compliance with protocols, Good Clinical Practice (GCP) guidelines, regulatory standards, and participant protection.

• Assess source data, essential documents, and site procedures for accuracy and thoroughness.

• Detect and address findings, risks, and necessary corrective actions.

• Maintain effective communication with investigators, site personnel, and study teams.

⛳️ Requirements

• Degree in life sciences, healthcare, clinical research, or equivalent relevant experience in clinical research.

• At least 2 years of experience as a Clinical Research Associate.

• Comprehensive understanding of clinical trial processes, regulations, and ICH Good Clinical Practice (GCP) standards.

• Familiarity with ICH Good Clinical Practice (GCP), clinical trial execution, and site monitoring requirements.

• Practical experience in site monitoring or site management suitable for the level of the position.

• Experience in executing site qualification, initiation, monitoring, and closeout tasks as needed.

• Proven ability to verify compliance with protocols, GCP, and regulatory requirements while ensuring participant protection.

• Willingness to travel as necessary (approximately 60%).

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career pathways.