Posted to MedZilla on 3/30/2017

Takeda Pharmaceuticals

US-MA, Summer Intern Global Regulatory Affairs Development Oncology 1700630-MZ


  • Assist members of the Regulatory Affairs Strategy with documentation, research and tasks as needed.
  • Executes regulatory activities for team members or projects in accordance with applicable regulations and guidelines under supervision.


  • Perform research into regulatory filings, regulations and other pertinent issues as requested
  • Compile and present to regulatory oncology organization on specific regulatory intelligence projects.
  • Assist with filing information into regulatory databases and documentation systems


  • A current student in an undergraduate or graduate program.
  • Basic science knowledge. Possesses strong oral and written communications, managing and adhering to timelines, negotiation skills, integrity and adaptability.
  • Demonstrates an interest in developing skills in the area of regulatory strategy and regulatory science.
  • Ability to work in a matrix environment and manage multiple priorities independently. Works well with others.

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