Join a Legacy of Innovation 110 Years and Counting!
Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 16,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. Under the Group’s 2025 Vision to become a “Global Pharma Innovator with Competitive Advantage in Oncology,” Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
Summary
The Director, Global Clinical Operations (GCO) Clinical Trial Operational Risk & Oversight (CTOR&O), will collaborate with the Head, Alliance & Vendor Oversight, CQM, and Process to build a GCO CTOR&O structure, ways of working, tools, and meaningful communication pathways with functional partners to support GCO risks. This individual will also lead and manage the GCO CTOR and Strategic Vendor Oversight teams, will partner with GCO leaders, subject matter experts (SMEs), and other functional area partners to ensure GCO risk management activities are executed and continuously monitored for effectiveness, efficiencies, and areas of improvement.
Responsibilities:
Clinical Trial Operational Risk (CTOR) Management:
Strategic Vendor Oversight (SVO):
Additional Collaboration Opportunities:
People Management:
Education Qualifications: (from an accredited college or university)
Travel:
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
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