Shelby Anderson
Senior Project Representative, DMPK-BA @ AbbVie
About
• 20 years of experience in ADME and pharmaceutical R&D from early drug discovery through to clinical trial execution and commercialization. • Technical knowledge across the ADME discipline, with particular depth in the biotransformation field. Responsible for > 75 radiolabeled mass balance/metID studies. • Experience with the Clinical Pharmacology/Biopharmaceutical package, including regulatory submissions & interactions. • Experience working with and managing external CROs to enable the ADME portfolio. • Evaluation of ADME properties as relevant to drug discovery and development, including SAR development; in vivo pharmacokinetics/toxicokinetics; bioanalysis, LC/MS and LBA; in vitro solubility, permeability, metabolic clearance, drug-interactions; metabolite profiling/ID and enzyme phenotyping
United States
Carmel
Pharmaceuticals
ADME, Drug Metabolism, Drug Discovery, LC-MS, GLP, CRO, In Vitro, Mass Spectrometry, Regulatory Submissions, Drug Development, Biomarkers, Pharmacokinetics, DMPK, Assay Development, Bioanalysis, Clinical Development, Pharmaceutical Industry, Protocol, Standard Operating Procedure (SOP), Pharmaceutics
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