
Analytical and detail-oriented Bio- Analytical Analyst with 4 years of progressive experience in development, validation, and integration in support of clinical and preclinical drug studies. Skilled in bio-analytical method development, sample extraction, and automation workflows for the quantification of drugs and metabolites in biological matrices. Experienced in applying principles of clinical chemistry, immunoassay optimization, and quality control within GLP, GMP, and FDA-regulated environments. Recognized for strong troubleshooting ability, technical precision, and collaborative teamwork with cross-functional Research & Development teams.