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 sites and coordinate across stakeholders to meet
• Serve as a key contact for clinical sites during site start-up, maintaining clear communication.
• Collaborate with PMs, CTMs, CRAs, Site Selection, and other teams to resolve issues.
• Identify risks to activation schedules and escalate to the PM as needed.

🎯 Requirements

• Bachelor’s in clinical research or related field, or equivalent experience.
• 2+ years as Project Coordinator or similar in biotech/pharma/CRO.
• Site Start-Up experience in global/multi-regional context.
• Understanding of essential document requirements and clinical trial docs.
• GCP knowledge and regulatory guidelines incl. Health Canada/FDA.
• Strong English; bilingual French/English or other EU/Asian language is a plus.

🎁 Benefits

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