Deborah Tien

About Deborah Tien

16 years experience in the biopharmaceutical industry; knowledge of US Food and Drug Administration regulations (including GCP, GLP, GMP)Results-driven project management professional with significant and progressive experience and expertise in project management best practicesSolid understanding of cross-functional R&D project management activities, encompassing areas such as Preclinical & Clinical Research, Regulatory Affairs, CMC, Marketing, Business Development, and Intellectual PropertyPMP Certified by the Project Management InstituteA leader, capable of influencing and motivating internal and external stakeholders to meet targets without having formal authorityAble to handle multiple responsibilities, priorities, tasks and projects simultaneously and of an increasingly complex natureWell-developed interpersonal skills with demonstrated ability to communicate effectively at all levels of an organization

Experience

1. Senior Global Program Manager, Strategy, Commercialization, and Innovation

   Amgen

   Oct 2018 — Present · Thousand Oaks, CA, US

Education

• Smith College

  B.A., Biological Sciences

• The Johns Hopkins University

  M.S., Biotechnology

Skills

• Gmp
• Molecular Biology
• Clinical Development
• Clinical Research
• Good Clinical Practice (Gcp)
• Project Management
• Intellectual Property
• Clinical Trials
• R&D
• U.s. Food and Drug Administration (Fda)
• Glp
• Manufacturing
• Biotechnology
• Cross-Functional Team Leadership
• Regulatory Affairs
• Pharmaceutical Industry
• Fda
• Drug Development
• Gcp
• Biopharmaceuticals