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Regulatory Affairs Associate – contract

  • Job type: Contract
  • Location: New Jersey
  • Salary: Competitive
  • Job reference: AC/NY/regulatory
  • Sector: EPM Scientific, Regulatory
  • Date posted: 20/07/2017
Regulatory Affairs Associate – contract

My client is looking to add a Regulatory Affairs Associate to the team for 6 months. The Regulatory Affairs Associate will be responsible for assisting the team with preparation/maintenance of regulatory submissions.

My client is a mid-size pharmaceutical company located in Northern NJ. The company recently entered a phase where they need all hands on deck. There are 2 open positions in the regulatory team.

Responsibilities
  • Oversee maintenance of regulatory records, documents, and files
  • Manage quality of eCTD submissions
  • Publish electronic applications
  • Ensure timely/accurate submissions to regulatory authorities
Requirements
  • 5+ years of regulatory experience in the pharmaceutical industry
  • Extensive experience with eCTD submissions
  • Proficient with Microsoft Office and Adobe Acrobat
  • Great communication skills
 


Apply now – you will be exposed to multiple submission types and there is potential to move into a more senior level role! 


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