Senior Clinical Research Associate - Remote

Overview

Bring your monitoring expertise to the forefront of innovation. We are looking for a Senior Clinical Research Associate (Sr. CRA) to join our Canada-based A-team (remote; with travel). As a Sr. CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice.

In Short

• Independently manage all aspects of monitoring for assigned clinical trials across study phases.
• Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
• Build strong site relationships, acting as a primary point of contact.
• Identify and resolve site issues, escalating as needed.
• Mentor and support junior CRAs, sharing knowledge and best practices.

Requirements

• Experience in clinical research monitoring.
• Strong understanding of GCP and regulatory requirements.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Willingness to travel throughout the United States.

Benefits

• Opportunity to work with a collaborative team.
• Mentorship opportunities for career growth.
• Flexible working arrangements.
• Involvement in impactful clinical trials.
• Supportive work environment focused on employee well-being.