MS office package
Well-established Pharmacovigilance and safety specialist offering more than 2+ years of expertise. Exceptional experience in safety and compliance inspections. Known for excellent quality review skills and knowledge in PV.
I was working on four peripheral and cardiac medical device trials and undertook pharmacovigilance activities such as collecting and tracking incoming adverse events (AE) and endpoint information; determining the initial or updated status of incoming events; database entry; coding AE and products; writing narratives; quality review; and literature-related activities in the Argus database. Prioritize and complete assigned trainings on time, ensuring that productivity and quality standards are met, and sign off on all assigned activities in accordance with applicable regulations, guidelines, Standard Operating Procedures (SOPs), and project requirements.
Data Entry
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Licensed Registered Pharmacist
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Licensed Registered Pharmacist