Senior Director Translational Patient Safety

1 month ago

Basking Ridge, United States Daiichi Sankyo, Inc Full time
  • With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 15,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people.
  • To succeed as global pharma innovator in oncology, a therapeutic area known for accelerated development and approval with smaller numbers of subjects exposed, Clinical Safety and Pharmacovigilance (CSPV) must be embedded in R&D as early as possible.
  • This led us to create the Translational Patient Safety Senior Director position, which will have unique exposure to Daiichi Sankyo's global drug portfolio from the Research stage to post marketing/lifecycle management.
  • Research and Nonclinical Development: For select drug candidates, especially ones addressing new targets or associated with new risks or linked to new risks, provide safety knowledge and input to Research in Tokyo based on the MOA and initial toxicological profile.
  • Surface expert knowledge on safety biomarkers that might be used in preclinical and clinical development by closely collaborating w Research and Precision Medicine.
  • Grow CSPV’s connection to toxicology (MSRL) and Precision Medicine beginning at the start of preclinical development.
  • 10 or more years of relevant experience in pharmacovigilance and related fields defined here required.
  • 7 or more years of experience within pharmacovigilance, clinical pharmacology, preclinical research, toxicology and/or biomarker validation (especially in industry) required.

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