Clinical Research Associate II

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 the smooth execution of studies.

• Carrying out data review and resolving 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

• 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 skills, with a strong focus on detail.

• Experience in monitoring phase I studies is required.

• Ability to work both independently and as part of a team in a fast-paced setting.

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

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

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellbeing resources.

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