About

I am a clinical trial operation and biospecimen data professional with over ten years of experience working in pharmaceutical and biotechnology environments across regulated manufacturing, quality control, and central laboratory operations. My work has focused on managing clinical biospecimen lifecycles and reconciling sample, shipment, and clinical datasets to maintain chain-of-custody integrity, data accuracy, and inspection readiness.

In my most recent role, I managed biospecimen data workflows across multiple clinical studies, investigating discrepancies between LIMS records, shipment manifests, and sponsor datasets while maintaining clear documentation and traceable audit trails. This work required resolving high volumes of reconciliation issues and ensuring study data remained complete, consistent, and audit ready.

I am currently on a professional sabbatical focused on expanding my technical capabilities in data analysis, including SQL, Excel-based analytics, and Power BI. My goal is to apply data-driven approaches to improve clinical data quality, biomarker data workflows, and operational visibility within clinical research organizations and biotech teams.

I am particularly interested in biomarker operations, clinical data management, and data-focused roles within biotech and clinical research organizations.