Clinical Research Associate

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

📋 Description

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

• Ensuring adherence to protocols, maintaining data integrity, and prioritizing patient safety throughout the trial process.

• Collaborating with investigators and site personnel to ensure seamless execution of the study.

• Performing data reviews and addressing queries to uphold the quality of clinical data.

• Assisting in the preparation and evaluation of study documentation, which includes protocols and clinical study reports.

⛳️ Requirements

• A bachelor's degree in a scientific or healthcare-related discipline.

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

• Comprehensive understanding of clinical trial processes, regulations, and ICH-GCP guidelines.

• Excellent organizational and communication abilities, with a keen attention to detail.

• Capacity to work both independently and collaboratively in a dynamic environment.

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, which may include medical, dental, and vision coverage.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and resources for wellbeing.

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