Posted to MedZilla on 3/30/2017


Takeda Pharmaceuticals

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


 
 

OBJECTIVES:
  • 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.

ACCOUNTABILITIES:

  • 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
Qualifications

EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:

  • 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.

We are driven to improve people's lives

www.takedajobs.com

Takeda is an EEO employer of minorities, women, disabled, protected veterans, and considers qualified applicants with criminal histories in accordance with applicable laws. For more information, visithttp://www.takeda.us/careers/EEO_Policy_Statement.aspx

No Phone Calls or Recruiters Please.


Schedule


Please visit our website at takedajobs.com

 
 


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  considered, please do so. Applications for all positions are subject to each employer's specific requirements.