Abdul Newaz
Pharmacovigilance - Clinical Safety Associate @Bristol Myers Squibb
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WORK HISTORY
Pharmacovigilance - Clinical Safety Associate @Bristol Myers Squibb
Lawrence, NJ, US
Reduced daily review time for over adverse event-related data points by 50% through the creation and implementation of Excel VBA Macros in compliance with regulatory requirements-Coordinate cross-functional meetings to implement Case Report Forms (CRF) targeting specific toxicities to enhance the safety profile of assets for various end utilities, including ICSRs, CSRs, HA Queries, and Aggregate Reports-Perform Data Management (DM) activities for in-house and outsourced trials: protocol review, CRF development, database set up activities, data validation process (including manual data review of listings), SAE reconciliation, managing database locks-Coordinated Clinical Research Organizations (CRO) data validation activities: data transfer specifications, data reconciliation, query generation and resolution, and participated in developing and implementing departmental standards and documents-Utilized data analytics tools like Tableau and Spotfire to create visualizations for in-depth analysis of aggregate clinical trial metadata, providing meaningful medical messaging across therapeutic areas (Immuno-Oncology, Cellular Therapy, Hematology, Oncology, Immunology, Fibrosis, Cardiovascular, Neurosciences).
EDUCATION
Brooklyn Technical High School
High School Diploma
New York Institute of Technology
Bachelor of Science - BS
ABOUT ABDUL NEWAZ
Pharmacovigilance Associate with a passion for patient safety and a strong foundation in…
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