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Associate Director, Clinical Pharmacology
1 month ago
Join a Legacy of Innovation 110 Years and Counting
Company is committed to diversity and inclusion. We are an equal opportunity employer including veterans and people with disabilities.
Summary
The Associate Director will be responsible for developing and implementing Clinical Pharmacology and Modeling & Simulation plans from FIH to post registration. Responsibilities include the development of Clinical Pharmacology and Modeling and Simulation plans, design and lead study teams to execute Clinical Pharmacology studies, conduct hands on population PK and PKPD analyses and participate in regulatory interactions and submissions representing the Clinical Pharmacology and Pharmacometrics/ Quantitative Clinical Pharmacology function. The incumbent will champion model-based drug development as an active team member of clinical and development teams.
Responsibilities
Education (from an accredited college or university) and Experience Qualifications One of the following is required: PhD in Pharmacology or Pharmaceutical Sciences or PharmD with a clinical pharmacology research fellowship and 4 years of relevant experience. 1 or more years industry experience required.Masters' degree with 6 years of relevant experience. 1 or more years industry experience required.Bachelor's degree with 8 years of relevant experience. 1 or more years industry experience required.
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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