This job is no longer available.
You can view related vacancies or set-up an email alert notification when similar jobs are added to the website using the buttons below.

 
The Opportunity

We're looking for a Regulatory Affairs Associate, working in the Pharmaceuticals & Medical Products industry in Madison, New Jersey, United States.

  • Prepares and reviews pre and post-approval submissions to the Food and Drug Administration, using governmental guidelines and regulations.
Details

The pay range we're offering is 40 to 42 per hour. This position may present an opportunity to go permanent.

Our Client

Our client is an award-winning clinical development company.  Improving lives globally with 20+ years’ experience in clinical research and strategic resourcing.  Elevating results with proven strategies, comprehensive solutions, and customized delivery models.

Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

Strong relationships provide you connections and access to great opportunities.  Industry expertise sets you up for success with helpful insights, career coaching, and professional training.  Grow and learn while you put your skills to work.  

Experience Required for Your Success
  • Bachelors degree in Chemistry or related field from an accredited college or university
  •  2-3 years of experience working with Regulatory CMC pre/post-approval submissions and agency responses
What Do You Think?

Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.

Not exactly? Join Our Talent Community, and we'll let you know of additional opportunities.