Adriana Lopez

Adriana Lopez has over 11 years of experience in bioanalytical analysis, including assay development, troubleshooting and validation, GLP regulations, timeline management for clinical studies, and technology transfer to and from Contract Research Organizations (CROs).  Adriana’s background includes five years of supervisory and project management experience, providing technical and regulatory oversight of client studies. Previously, she worked at Tandem Labs, A LabCorp Company, where her primary responsibility was to oversee the development and validation of clinical and biomarker assays and the analysis of clinical and nonclinical samples for all therapeutic programs in a GLP laboratory. In addition, she was responsible for training personnel (QC/QA, PMs, and analysts) on how to use the Watson LIMS system.  

Before joining Tandem Labs, Adriana was employed at Amylin Pharmaceuticals, where she designed, optimized, validated, and performed custom and commercially available ELISAs on various platforms (Luminex, M5, and MSD).  In addition, she was responsible for interfacing with contract laboratory facilities to ensure smooth lab-to-lab transfer of laboratory methods. In this role, she was responsible for training CRO personnel.  Once the technique was transferred successfully, Adriana oversaw the scientific progress toward program goals. She obtained a Bachelor of Science from California State University of Long Beach, CA.