Clinical Regulatory Affairs Submissions

Boston, MA

Job ID: 128701 Industry: CLINICAL


Clinical Regulatory Affairs Submissions

Project Description:                                                     

Our client is currently in the process of hiring a Regulatory Affairs SME to help with submissions to the FDA.  This person will be working on NDA’ s and supplemental submissions.  

Day to Day Responsibilities:

Currently the client does not have enough full time staff to handle the work load.  They are looking for someone to come on site and help conduct submission work with NDA’ s and supplemental submissions.  The consultant chosen for this roll will be expected to work with little to no direction and have significant experience working with pharmaceutical submissions in the past. 

Required Skills:

Regulatory Affairs



Job Type: Contract

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