Study Manager
Core
End-to-end study management for clinical trials in Canada, ensuring delivery to agreed quality, timelines, and budget while ensuring regulatory compliance.
Role type
Mid-level clinical study manager (Canada-based)
Builds
Clinical studies for vaccines and medicines
Domain
Biopharmaceuticals / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical operations, study management, pharmaceutical project management, ICH-GCP, Health Canada regulations, site and patient management, protocol development, risk mitigation
Preferred skills
Global pharma or CRO environment experience, North American clinical trial requirements, matrixed team collaboration, mentoring
Technologies
Clinical trial management tools, Microsoft Office
Responsibilities
Lead planning, set-up, execution, and close-out of clinical studies; coordinate cross-functional teams; oversee site and patient management; ensure regulatory compliance; contribute to study documentation; identify and mitigate operational risks; support team onboarding
Seniority
Mid-level, hands-on IC
