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 activation timelines and coordinate across stakeholders to hit milestones.
• Serve as main contact for clinical sites during start-up, ensuring priorities align with timelines.
• Collaborate with PMs, CTMs, CRAs, Site Selection, and other teams to coordinate activities and
• Identify risks to activation schedules and escalate to the PM as needed.

🎯 Requirements

• Bachelor’s in clinical research or related field, or equivalent experience.
• A specialized graduate diploma in drug development is an asset.
• At least 2 years as Project Coordinator or similar clinical research role in biotech/pharma/CRO.
• Site Start-Up experience in global or multi-regional environment.
• Solid understanding of essential document requirements and trial documentation processes.
• GCP knowledge and regulatory guidelines (Health Canada, FDA).

🎁 Benefits

• Permanent, full-time employment.
• Flexible work schedule.
• Company benefits package.
• Ongoing learning, training, and development opportunities.
• Career growth and advancement.
• Collaborative, international work environment.