Director Clinical Site Management Monitoring
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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 good 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. #J-18808-Ljbffr
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