Experience

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  Pusan national university hospital

  Mar 2009 - Jul 2010

  Hospital pharmacist & research pharmacist in regional pharmacovigilance research center

  Clinical hospital pharmacist: - Engaged in medication management, patient care services, and educational consultationsClinical evaluator at the Pusan National University Regional Pharmacovigilance Research Center: - Collected post-marketing adverse drug reaction (ADR) case reports- Evaluated the clinical-pharmacological aspects of the case history regarding potential drug safety- Assessed the likelihood of suspected ADR case reports by using WHO–Uppsala Monitoring Center causality categories Show less

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  Regeneron

  Jun 2021 - Aug 2021

  Pharmacoepidemiology intern

  - Supported the creation of a database to monitor adverse outcomes associated with drug use during pregnancy within a registry, fulfilling a post-marketing requirement for regulatory agencies- Conducted systematic and targeted epidemiologic literature reviews to support post-marketing regulatory research- Developed epidemiologic study designs and protocols, and conducted a study examining the natural history and clinical outcomes in patients with lipodystrophy using RWD

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  Regeneron

  Oct 2021 - Oct 2022

  Pharmacoepidemiologist

  - Actively contributed to pharmacoepidemiologic activities for assigned development compound- Contributed to communication and dissemination of results to internal stakeholders

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  University of pittsburgh school of medicine

  Jan 2024 - Jun 2024

  Medical data scientist

  - Developed pharmacoepidemiologic study designs, encompassing health resource utilization, drug utilization patterns, and comparative safety and effectiveness research- Performed and handled pharmacoepidemiologic research projects involving the analysis of multiple types of real-world data (RWD), such as administrative claims and electronic health records (EHR)- Contributed to the development and implementation of innovative statistical analytic methods- Developed conference abstracts/presentations/manuscripts based on observational studies to disseminate real-world evidence (RWE) Show less

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  Regeneron

  Jul 2024 - now

  - Manage the generation of real-world evidence (RWE) in support of the regulatory queries and submissions, design and conduct of regulatory required epidemiologic studies (PASS/PMR, PAES, REMS, DUS)- Actively contribute to other pharmacoepidemiologic activities for assigned marketed/development compound(s) or TAs, including Risk Management Plans, Benefit-Risk analyses, post-approval safety studies that may not be required by a regulatory authority, signal management, responses to regulatory agency queries, regulatory filings, and safety surveillance Show less

  • Senior Manager in Pharmacoepidemiology

    Dec 2024 - now

  • Pharmacoepidemiologist

    Jul 2024 - Dec 2024