Senior Project Coordinator

📋 Description

• Coordinate site activation activities from site selection through activation, ensuring timelines
• Prepare investigator sites for clinical trials by reviewing, collecting, approving, filing, and
• Establish site activation timelines with selected sites and coordinate activities across
• Serve as a key point of contact for clinical sites during site start-up, maintaining clear
• Collaborate with Project Managers, Clinical Trial Managers, CRAs, Site Selection teams, and other
• Identify risks to site activation schedules and escalate issues to the Project Manager promptly.

🎯 Requirements

• Bachelor’s degree in clinical research or related field, or equivalent experience.
• 2+ years as a Project Coordinator or in clinical research in biotech/pharma/CRO.
• Site Start-Up experience in global/multi-regional environment.
• Understanding of essential document requirements and trial documentation processes.
• GCP knowledge and regulatory familiarity (Health Canada, FDA).
• Strong English communication; bilingualism or additional language skills are assets.

🎁 Benefits

• Permanent, full-time employment.
• Flexible work schedule.
• Company benefits package.
• Ongoing learning, training, and professional development opportunities.
• Opportunities for career growth and advancement.
• Collaborative international work environment with global trial impact.