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 particularly interested in biomarker sample operations, process improvement, and data-focused roles within biotech and clinical research organizations.