Results-oriented pharmacovigilance professional with more than five years of experience in preparing elaborated and accurate risk management plans (RMP), Health authority assessment reports (HAAR), safety evaluation, response documents, safety profile for PSURs and Clinical safety review documents. Expert at delivering high-quality work within tight deadlines. Effectively and proactively engaged in regulatory colleagues regarding Health authority requests/assignments/documents.
Talented individual collaborates with cross-functional teams for accuracy and clarity of scientific content.
Detail-oriented team player with strong organizational skills. Ability to handle multiple projects simultaneously with a high degree of accuracy.
Authoring/Review of Risk Management Plans and HA/RMS/CMS documents
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