Lead clinical site management and monitoring for Astra Zeneca, with expertise in study delivery, ICH-GCP, and field-based work in Ontario preferred.
The Director, Site Management & Monitoring oversees committed clinical interventional study delivery within resources, budgets, and timelines. This leadership role manages staff resources, study sites, and country-level targets. It requires project management, line management, monitoring knowledge, and regulatory understanding.
Key Responsibilities: Lead dedicated groups and develop direct reports
Plan study resources, budgets, timelines, and workload
Oversee site qualification, initiation, supervision, and closure
Maintain complete, timely, inspection-ready e TMF documentation
Review monitoring reports and perform accompanied site visits
Requirements: Bachelor degree in a related subject area
Minimum five years in Development Operations or related fields
Proven project management and line management experience
Very positive knowledge of clinical study processes and ICH-GCP
Ability to travel nationally and internationally
Apply clinical operations leadership, monitoring expertise, and people management to deliver quality studies for Astra Zeneca across Canada.

📌 Director clinical site management monitoring (Quebec City)
🏢 AstraZeneca
📍 Quebec City