Ken Joerg is a seasoned professional with over 10 years of experience in adverse event reporting, including both pre and post-marketing activities, and has actively participated in regulatory inspections. Currently serving as the Director Drug Safety Surveillance Team Lead for Anti-Infectives and Vaccines at Pfizer Pharmaceuticals since 2009, Ken manages a team responsible for preparing adverse event reports for submissions to regulatory authorities. Prior to this, Ken held the position of Director of Drug Safety Surveillance at Wyeth Pharmaceuticals from 1998 to 2009 and worked as a Staff Pharmacist at Thomas Jefferson University Hospital from 1984 to 1998. Ken holds an MBA in General Business from Drexel University and completed a PharmD at Shenandoah University, along with a BS in Pharmacy from the University of the Sciences in Philadelphia.
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