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Your Search Term(s): Clinical » Regulatory Affairs » Writer
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Company Job Title Location Posting Date
Aerotek Clinical  Regulatory Affairs Specialist Cambridge, Massachusetts 12/30/2015
...Development and driving of submission timelines: will be pushing internal teams to review Managing vendor responsible for the review, qc, and content check of FDA submissions Collaborating with medical writer & CMC formulations experts

Job Posting Search Results 01 - 01 of 01
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