Talented drug safety associate with a strong background in adverse event reporting.
Member of Kappa Kappa Gamma
Deans List 2003-2005
2011-2013 - Drug Safety Associate, Biologics Two
2007-2011 - Drug Safety Associate, Over the Counter Products
2006-2007 - Drug Safety Associate, Legal
Responsible for the case processing of adverse event reports following company standard operating procedures, internal business practices and regulatory guidance documents to ensure compliance with worldwide safety regulations and corporate policies. Triage of incoming cases to prioritize for daily work flow management, confirmation of case registration/committal information by Global Case Receipt staff, completion of remaining case processing including labeling and narrative writing as appropriate, liaison with global case receipt and or physician staff to clarify information required for case processing.
2007-2013: Facilities Committee
2010-2013: United Way Committee
Received and applied vendor date from study sites participating in study drug trials.
Health care consultant at Wyeth Pharmaceuticals for the highly confidential Special Task Force.
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