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
- Solid documentation, tracking, and operational coordination skills

Apply oncology study coordination, systems stewardship, vendor management, and publication workflow expertise across compliant evidence generation activities.

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