Lead global oncology clinical operations at Daiichi Sankyo, directing company-sponsored studies and medical affairs research across international teams and partners.
As Director, Company Sponsored Studies, you will guide interventional and non-interventional studies within Global Oncology Medical Affairs. The work spans operational planning, protocol development support, study execution, final reporting, and risk management. You will coordinate Medical Affairs, Clinical Operations, Regulatory Affairs, Safety, Data Management, Statistics, Quality, and external partners.
Key Responsibilities: Lead global oncology study planning, execution, delivery, and close-out
Drive cross-functional global study teams as Global Study Lead
Direct CRO and vendor performance, risks, budgets, and milestones
Support protocols, start-up activities, execution,



and final reporting
Improve clinical operations processes, systems, SOPs, and quality standards
Requirements: Master’s degree in Life Sciences required; PhD or PharmD preferred
Minimum eight years of international GxP clinical operations experience
Experience leading global interventional and non-interventional clinical studies
Excellent knowledge of GCP, regulations, vendors, and study management
Skilled English and strong leadership, communication, and stakeholder skills
Bring global study leadership, oncology operations expertise, and GCP knowledge to Daiichi Sankyo’s Medical Affairs organization.

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📌 Director Global Oncology Clinical Operations (Ontario)
🏢 Daiichi Sankyo
📍 Ontario