Project Manager, Vendor Management

📋 Description

• Lead or support initiation, planning, execution, monitoring, control, and closeout of clinical
• Coordinate site activation, feasibility, initiation, documentation, training, recruitment
• Manage internal resources, prioritize activities, ensure quality deliverables, and support study
• Monitor performance, reconcile trackers, and contribute to corrective actions and risk management.
• Prepare operational plans, study deliverables, regulatory submissions, and TMF quality reviews for
• Collaborate with Data Management and other teams to support CRF compliance and data review.

🎯 Requirements

• Bachelor’s degree in a relevant scientific or clinical research field.
• At least 3 years in a comparable clinical study management role in pharma/biotech/CRO.
• At least 2 years coordinating clinical trial management activities.
• Strong knowledge of GCP, ICH, FDA requirements, and Canadian regulations.
• Experience managing small to mid-sized projects with a structured PM approach.
• Vendor management experience is highly valuable.

🎁 Benefits

• Permanent, full-time employment.
• Flexible work schedule and fully remote option from Canada (Montreal office possible).
• Comprehensive benefits: medical, dental, vision; RRSP; vacation/personal days.
• Virtual medical clinic access and transportation rebates.
• Social activities and ongoing learning with career growth opportunities.
• Collaborative, innovative, science-driven environment with international teams.