Experience

Acorda Therapeutics, Inc.

• United States
• Biotechnology Research
• 100 - 200 Employee

• Drug Safety Specialist

  • Jun 2015 - Present



Bayer GPV

• Montville, NJ

• Senior Safety Data Specialist

  • Aug 2011 - Present



Johnson & Johnson

• United States
• Hospitals and Health Care
• 700 & Above Employee

• Drug Safety Specialist

  • Feb 2015 - Apr 2015



IQVIA

• United States
• Hospitals and Health Care
• 700 & Above Employee

• Associate Operations Specialist

  • Apr 2011 - Aug 2011

  Investigate, evaluate, process, and enter, into ARISg database, individual serious and non-serious adverse event case reports for a Phase III clinical study. Responsible for QC of serious case reports, narrative generation, upgrade and case modifications following rigid medical review for a Phase III clinical study. Update InForm clinical database with new queries and modify as necessary. Investigate, evaluate, process, and enter, into ARISg database, individual serious and non-serious adverse event case reports for a Phase III clinical study. Responsible for QC of serious case reports, narrative generation, upgrade and case modifications following rigid medical review for a Phase III clinical study. Update InForm clinical database with new queries and modify as necessary.



U.S. Navy Reserve

• United States
• Armed Forces
• 700 & Above Employee

• Hospital Corpsman 1st Class (FMF)

  • Mar 1992 - Aug 2011

  Multiple stateside and international mobilizations and activities providing routine and emergency medical care to military personnel and civilians. Two combat tours in support of Operation Iraqi Freedom (2003/2008-2009). Multiple stateside and international mobilizations and activities providing routine and emergency medical care to military personnel and civilians. Two combat tours in support of Operation Iraqi Freedom (2003/2008-2009).



Celgene

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Drug Safety Specialist

  • Oct 2009 - Mar 2011

  Investigate, evaluate, process, and enter, into ARISg database, individual serious and non-serious adverse event case reports (clinical trials, IIT, post-market, literature). Responsible for QC of serious and non-serious case reports, narrative generation, triage, upgrade and case modifications following rigid medical review (clinical trials, IIT, post-market, literature). Investigate, evaluate, process, and enter, into ARISg database, individual serious and non-serious adverse event case reports (clinical trials, IIT, post-market, literature). Responsible for QC of serious and non-serious case reports, narrative generation, triage, upgrade and case modifications following rigid medical review (clinical trials, IIT, post-market, literature).



i3 Drug Safety

• Safety Coordinator, RN

  • Sep 2007 - Aug 2009

  Registered Nurse responsible for medical record/sponsor document review and associated input and reporting of AE/SAE into proprietary and ARISg databases with strict adherence to FDA and international reporting regulations (post-market). Responsible for receipt of consumer and health care provider reports with associated data entry into AE/SAE databases (post-market). Registered Nurse responsible for medical record/sponsor document review and associated input and reporting of AE/SAE into proprietary and ARISg databases with strict adherence to FDA and international reporting regulations (post-market). Responsible for receipt of consumer and health care provider reports with associated data entry into AE/SAE databases (post-market).