Senior Project Coordinator

📋 Description

• Coordinate site activation activities from site selection through activation, ensuring timelines
• Prepare investigator sites for clinical trials by reviewing and tracking essential regulatory
• Establish site activation timelines and coordinate activities across stakeholders to meet
• Serve as a key contact for clinical sites during start-up, ensuring timelines stay aligned.
• Collaborate with Project Managers, Clinical Trial Managers, CRAs, Site Selection teams, and others
• Identify risks to activation schedules and escalate to the Project Manager as needed.

🎯 Requirements

• Bachelor’s degree in clinical research or related field, or equivalent experience.
• 2+ years as a Project Coordinator or equivalent in biotech/pharma/CRO.
• Site Start-Up experience in global/multi-regional settings.
• Solid understanding of essential document requirements and clinical trial documentation.
• Good Clinical Practice (GCP) and regulatory knowledge (Health Canada, FDA).
• Strong written/spoken English; French or other European/Asian language a plus.

🎁 Benefits

• Permanent, full-time employment.
• Flexible work schedule.
• Company benefits package.
• Ongoing learning, training, and professional development.
• Opportunities for career growth in an international environment.
• Collaborative atmosphere with global impact on clinical trials.