Study Start-Up Project Manager

📋 Description

• Oversee global study start-up activities for clinical trials
• Ensure regulatory submissions and site activation are completed efficiently
• Act as main contact for start-up operations with sponsors
• Support quality, compliance, and trial execution at multiple sites

🎯 Requirements

• Bachelor’s degree in science, healthcare, or related field
• Minimum 5 years in study start-up within a CRO
• Experience with Health Canada submissions and ethics committees
• Strong knowledge of ICH guidelines and local regulatory requirements
• Experience managing trial documentation, site activation, and regulatory workflows
• Fluency in English; French is a plus

🎁 Benefits

• Competitive compensation in local currency (CAD)
• Bonus program opportunities
• Sign-on bonus and equity opportunities
• Flexible work environment
• Comprehensive medical and life insurance
• Voluntary pension plan