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 Solid 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 (Winnipeg)
🏢 Brunel
📍 Winnipeg