Lead oncology and biopharmaceutical evidence delivery for ESR studies in Canada, coordinating clinical operations, research agreements, and cross-functional execution.
As Evidence Delivery Manager, Medical Evidence, you will oversee ESR studies within assigned therapeutic areas across the Oncology and Biopharmaceuticals Business Units. Reporting to the Director, Medical Evidence in Canada, you will coordinate stakeholders, Principal Investigators, and study teams. Your work supports compliant delivery against time, cost, and quality objectives through project management, study systems, documentation, and budget coordination.
Key Responsibilities: Evaluate operational feasibility during triage and proposal reviews
Coordinate protocols, amendments, and stakeholder approvals
Maintain studies and performance assessments in Veeva Clinical Vault




Lead confidentiality and research agreement execution
Manage study budgets, invoices, trackers, and stakeholder updates
Requirements: Bachelor’s degree in science required; advanced degree preferred
Experience in project or clinical study management
Knowledge of clinical trials, drug development, and GCP/ICH guidelines
Robust communication in cross-functional matrixed environments
Autonomy, organization, prioritization, and attention to detail
Apply clinical study management, stakeholder communication, and evidence delivery expertise across Canadian ESR programs and therapeutic areas.

📌 Medical Evidence Delivery Manager (Mississauga)
🏢 Brunel
📍 Mississauga