Director Clinical Site Management Monitoring (Quebec City)

Director Clinical Site Management Monitoring (Quebec City)

22 Oct
|
AstraZeneca
|
Quebec City

22 Oct

AstraZeneca

Quebec City

Lead clinical site management and monitoring for AstraZeneca, 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 eTMF 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 AstraZeneca across Canada.

📌 Director Clinical Site Management Monitoring (Quebec City)
🏢 AstraZeneca
📍 Quebec City

Reply to this offer

Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.

Subscribe to this job alert:

Get the latest job offers by email for: director clinical site management monitoring (quebec city) / quebec city

Subscribe to this job alert:

Get the latest job offers by email for: director clinical site management monitoring (quebec city) / quebec city