Covance

Regulatory Submissions Associate

MX
Job Number
2017-15421
Job Category
Clinical Operations
Position Type
Full-Time

Job Overview

Get ready to redefine what’s possible and discover your extraordinary potential at Covance. Here, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning. 

 

 

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 II to join our location in Mexico City!

 

The Regulatory Submissions Associate II 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 II interacts with Regulatory Authorities and with clients to support regulatory activities.

 

Responsibilities/Duties:

  • 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

Education/Qualifications

  • Bachelor’s Degree in Life Sciences or equivalent

Experience

 

  • 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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