Greater Chicago Area
As a Research Assistant at Loyola University Chicago's Parkinson School of Health Sciences and Public Health, I translate complex epidemiology findings into actionable insights for clinical stakeholders and community partners. My work includes statistical analysis of health trends, stakeholder engagement through interviews, and co-authoring manuscripts currently in the publication process. Pursuing an MPH in Epidemiology at Loyola University Chicago, I aim to deepen my expertise in biostatistics, real-world evidence (RWE), and public health research. With a PharmD and clinical pharmacy background in oncology, I bring a unique perspective to multidisciplinary collaborations, focusing on evidence-based strategies and scientific communication to drive meaningful public health outcomes.
- Translated complex epidemiology findings from large-scale U.S. datasets into actionable insights for non-academic clinical stakeholders and community partners. - Spearheaded statistical analysis on health trends and risk patterns to guide evidence-based public health strategy. - Led 25+ stakeholder interviews for a funded I-CORP project, strengthening academic–community partnerships through effective scientific communication. - Presented at conferences (2) and co-authored manuscripts in process of publication (3).
- Developed components of Statistical Analysis Plans (SAPs), including dataset definitions and table shells, ensuring high-quality data integrity for publication-track research. - Executed advanced statistical modeling (Regression, Longitudinal, and Trend Analysis) using SAS to analyze mental health outcomes in the U.S. population. - Co-authored a manuscript and an abstract on suicide trends, bridging the gap between raw data and public health literature.
Moved to the US
Facilitated non-promotional, peer-to-peer scientific interactions with leading oncologists to discuss therapeutic advancements in solid tumors and hematology. Identified and communicated actionable field insights regarding patient access barriers and treatment patterns to internal stakeholders. Provided deep-dive analysis on mechanisms of action (MOA) and clinical data for advanced oncology therapeutics. Served as the clinical pharmacy lead for FACT Accreditation, establishing rigorous standards for cellular therapy and high-complexity BMT protocols. Developed and conducted 15+ high-level medical education sessions for HCPs, focusing on the safety profiles and clinical efficacy of emerging agents. Evaluated real-world evidence (RWE) and clinical trial data to drive oncology formulary development and optimize institutional cost-offsets. Spearheaded pharmacovigilance activities and safety reporting for 100+ ADRs, ensuring regulatory compliance and proactive toxicity management. Authored institutional monitoring pathways for monoclonal antibodies to minimize infusion-related reactions and enhance patient safety.
Interpreted complex Phase II/III clinical trial data to provide scientific dialogue aligned with evolving global standards of care. Supported cross-functional medical activities across genitourinary, BMT (CAR-T), and solid tumor therapeutic areas to foster investigator relationships. Conducted structured medical presentations within professional development settings, translating clinical data into actionable bedside insights. Developed proactive monitoring pathways for monoclonal antibodies to identify and mitigate Cytokine Release Syndrome (CRS). Facilitated patient evaluation and access to IV home infusion and specialized infectious disease programs within oncology care.
- Completed advanced clinical pharmacy training in general medicine, pediatrics, surgery, and psychiatry. - Engaged in multidisciplinary ward rounds, providing therapeutic recommendations based on clinical guidelines. - Assisted in pharmacovigilance activities, ensuring compliance with reporting requirements for adverse drug reactions. - Delivered 100+ structured scientific case discussions to healthcare providers, demonstrating expertise in medical storytelling and evidence synthesis. - Conducted all research activities in strict accordance with Good Clinical Practice (GCP) and institutional credentialing requirements.