Provide analytical chemistry support to projects across the clinical drug development pipeline
Execute test method protocols for in-vitro biopharmaceutics team that includes but not limited to thermodynamic solubility measurement, USP dissolution, precipitation and flux assays
Prepare analytical solutions and biorelevant media for in-vitro experiments, including accurate weighing, potency corrections, buffer preparation, and appropriate handling of active pharmaceutical ingredients
Analyze study samples by HPLC and UV-vis, including calibration standard preparation, sample processing, and quantitation of drug concentration from in-vitro studies
Perform first-pass review of dissolution, solubility, and analytical data, identifying anomalous results (e.g., carryover, precipitation, coning, filtration loss) for scientific follow-up
Document findings in electronic lab notebooks and technical reports in accordance with ALCOA data integrity principles
Support routine laboratory operations, including equipment readiness, consumables, safe lab practices, and scheduling instruments
Adapt experimental execution and prioritization to shifting project needs, balancing scientific rigor with resource efficiency and study objectives