Associate Director, Clinical Science

3 days ago

Bernards, United States Daiichi Sankyo, Inc. Full time
p>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 120 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.Oversees typically a single non-pivotal trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Drafts development plans, protocol profiles, and sections of submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to Clinical Operations. Represents Clinical Development on Project Teams.Education Qualifications (from an accredited college or university)

  • Master's Degree or equivalent preferred or
  • PharmD or equivalent preferred or
  • PhD or equivalent preferred
  • Postgraduate training in TA or related specialty, or equivalent preferred

Experience Qualifications

  • 4 or More Years with PharmD, PhD and relevant clinical experience preferred
  • 7 or More Years with Master’s degree and relevant clinical experience preferred

Travel

Ability to travel up to 30% In-house office position that may require travel (global).

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