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 reviewsCoordinate protocols, amendments,



and stakeholder approvalsMaintain studies and performance assessments in Veeva Clinical VaultLead confidentiality and research agreement executionManage study budgets, invoices, trackers, and stakeholder updatesRequirements: Bachelor’s degree in science required; advanced degree preferredExperience in project or clinical study managementKnowledge of clinical trials, drug development, and GCP/ICH guidelinesStrong communication in cross-functional matrixed environmentsAutonomy, organization, prioritization, and attention to detailApply clinical study management, stakeholder communication, and evidence delivery expertise across Canadian ESR programs and therapeutic areas.#J-18808-Ljbffr

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