Coordinate oncology evidence generation studies using Veeva Clinical Vault, Airtable, and detailed operational tracking. Support secondary and primary studies across global and local teams.
As Project Coordinator, you will support O2R Study Leads within the Oncology Business Unit Medical organization. Your work centers on secondary data studies, with complementary primary and hybrid study support. You will coordinate contracting, vendors, finance operations, documentation, TMF activities, and publication review workflows. The role sits within Medical Excellence, Strategy and Operations and requires cross-functional collaboration.
Key Responsibilities: Support secondary data, primary, and hybrid study conduct
Maintain study milestones and attributes across systems
Coordinate contracts, vendors, requests, and amendments
Manage purchase orders,



invoices, cost centers, and spend
Coordinate publication reviews, author feedback, and signoffs
Requirements: Bachelor’s degree in business, life sciences, or related field
Minimum one year in pharmaceutical or regulated medical products industry
Working knowledge of Evidence Generation Studies and TMF
Experience with Veeva Clinical Vault, ABACUS, or Airtable
Robust documentation, tracking, and operational coordination skills
Apply oncology study coordination, systems stewardship, vendor management, and publication workflow expertise across compliant evidence generation activities.

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📌 Oncology Evidence Generation Coordinator (Ontario)
🏢 Brunel
📍 Ontario