Senior Clinical Research Associate / Clinical Research Associate II - Remote

Overview

The Senior Clinical Research Associate (CRA) is responsible for monitoring clinical studies at investigative sites, ensuring compliance with protocols and regulations.

In Short

• Monitor clinical trials at investigative sites.
• Work autonomously to meet quality standards.
• Focus on dermatology research.
• Conduct site qualification and monitoring visits.
• Prepare reports and maintain documentation.
• Build relationships with investigators and site staff.
• Ensure compliance with ICH/GCP standards.
• Travel to research sites approximately 65% of the time.
• Home-based position with teleworking allowance.
• Permanent full-time position with benefits.

Requirements

• B.Sc. in a relevant field or equivalent experience.
• 2 to 5 years of clinical monitoring experience.
• Good knowledge of ICH/GCP standards.
• Strong verbal and written English communication skills.
• Ability to prioritize and work under pressure.
• Excellent judgement and problem-solving skills.
• Proficiency in Microsoft Office.
• Experience in dermatology is an asset.

Benefits

• Permanent full-time position.
• Vacation and health allowance.
• Home-based position with teleworking allowance.
• Ongoing learning and development opportunities.