Associate Director - Pharma, Global Regulatory Affairs, Biomedical Research, Clinical Trials
Posted by: ProNetworkMedia
Posted date: 2010-May-17
Location: Boonton, New Jersey area
We are looking for an Associate Director to make an immediate impact and perform management of global regulatory drug activities, perform submission and approvals, perform management of regulatory activities, work with regulatory activities, and other related duties
REQUIRED
Candidates must have 10+ years pharma, biomedical research and clinical trials
Candidates must have 5+ years regulatory affairs
Candidates must have an advanced degree biomedical research