1+ months
2018-05-292018-08-29

Associate

DLA Piper
Washington, DC








The DC office of DLA Piper is seeking a mid-level candidate to join our FDA regulatory practice.  The candidate must have substantial experience in pharmaceutical and/or medical device regulatory issues, including but not limited to one or more of the following areas: the Hatch-Waxman and Biosimilars regulatory schemes (approval criteria, labeling, and exclusivities); product development and clinical trials; regulation of advertising and promotion for medical products (including fraud and abuse issues); cGMP/QSR compliance and enforcement;  device classification, clearance and approval processes.  Ideal candidates will also have experience in FDA dispute resolution procedures and administrative (APA) litigation.  We seek candidates with immediately transferable skills and a strong academic background from a nationally recognized law school. Exceptional written and oral communication skills are a must. We offer competitive salaries and benefits.
 
Please apply on line if you are a direct applicant.  If you have a request for an accommodation during the application process or if you have any questions about the process, please contact Jessica Patton at jessica.patton@dlapiper.com; however, please submit all materials online.  Please add noreply@dlapipertalent.com to your list of safe senders.
 
Search Firms - Per the terms of our agreement, all candidates must be submitted through our agency portal for consideration.










JD and substantial experience in pharmaceutical and/or medical device regulatory issues.

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Associate

DLA Piper
Washington, DC

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