Resumes
Resumes

Assistant Director | Manager With Expertise In Pharmacovigilance | Drug Safety, Risk Management And Computer Systems
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Seasoned professional in drug safety, pharmacovigilance and risk management at Open to new opportunities in drug safety, pharmacovigilance and risk management, Associate Director | Consultant | Pharmacovigilance at Full time, contract and consultant opportunities, Founder || Assistant Director | Manager | Pharmacovigilance at Visionaries in Pharmacovigilance
Location:
Greater Philadelphia Area
Industry:
Pharmaceuticals
Work:
Open to new opportunities in drug safety, pharmacovigilance and risk management - Newtown Square, PA 19073 USA since Jan 2012
Seasoned professional in drug safety, pharmacovigilance and risk management
Full time, contract and consultant opportunities since Jan 2012
Associate Director | Consultant | Pharmacovigilance
Visionaries in Pharmacovigilance - Greater Philadelphia Area since 2012
Founder || Assistant Director | Manager | Pharmacovigilance
Schering-Plough Research Institute 2008 - 2010
Signal Detection Specialist
Seasoned professional in drug safety, pharmacovigilance and risk management
Full time, contract and consultant opportunities since Jan 2012
Associate Director | Consultant | Pharmacovigilance
Visionaries in Pharmacovigilance - Greater Philadelphia Area since 2012
Founder || Assistant Director | Manager | Pharmacovigilance
Schering-Plough Research Institute 2008 - 2010
Signal Detection Specialist
Education:
Drexel University - College of Business and Administration
MBA, Management Philadelphia College of Pharmacy and Science
BSc, Pharmacy
MBA, Management Philadelphia College of Pharmacy and Science
BSc, Pharmacy
Interests:
Drug Safety
Pharmacovigilance
Risk Management
Signal detection and evaluation
Pharmacovigilance plans
Risk Management Plans
Risk MaPPs
Clinical Research
Clinical Trials
Medical Writing, Review, Editing
Periodic Risk Benefit Evaluation Reports (PBRERs)
Periodic Safety Update Reports (PSURs)
Clinical Study Reports (CSRs)
Quarterly Study Reports (QSRs)
Annual Study Reports (ASRs)
US PADER reports
Published Author
Regulatory Affairs
Global Regulatory Compliance
FDA, EU. EMEA, Eudravigilance
SOP evaluation and creation
FDA Inspections
EU, MHRA Inspections
Inspection preparedness training
AE database selection, validation and project managment
Data review, analysis and evaluation
Adhoc AE requests from Healh Authorities
PV training and development
Employee selection, training and evaluation
Review and evaluation of medical literature
Persuasive Presentations
Budgeting and Resource Planning
Honor & Awards:
DIA Outstanding Contributor to Clinical Safety and Pharmacovigilance Special Interest Community
Aventis Pasteur Significant Contributor to Pharmacovigilance Systems Implementation