Regulatory Submissions Specialist

Job Location(s) MX
Job Number
Job Category
Clinical Operations
Position Type

Job Overview

Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients—and your career.


Covance is currently hiring a Regulatory Submissions Associate to join our location in Mexico City!


The Regulatory Submissions Associate is responsible for providing support to regulatory managers and others for the timely submission of information to Regulatory Authorities in support of investigational and marketed products.The Associate interacts with Regulatory Authorities and with clients to support regulatory activities.



  • Proactively interacts with other Covance groups and with clients to provide guidance regarding Regulatory Authority requirements and project timelines.
  • Is responsible for preparing documents to the required standard.
  • Is responsible for staying up to date and maintaining awareness of current regulatory standards related to submissions for drug and biologic products. 
  • Proactively liaises with clients on regulatory submission issues


  • Bachelor’s Degree in Life Sciences or equivalent



  • 2 years in the pharmaceutical industry
  • Experience in Drug Development or Regulatory Affairs preferred
  • Excellent communication skills, organization and planning skills and attention to detail


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