• High learning agility and a keen ability to derive and efficiently test ADME and DMPK hypotheses
• Strong working knowledge in fundamental pharmaceutics, pharmacokinetics and ADME principles across a variety of therapeutic modalities
• Understanding of contemporary pharmaceutical regulatory guidance and expectations
• Skills to integrate internal and external laboratory and other experimental resources through high quality scientific associations
• Agile interrogation of diverse data (e.g., in silico, in vitro, in vivo) to derive mechanistic understanding of drug action and performance characteristics

• Lead and innovate in a multidisciplinary collaborative environment with primary responsibility for ADME studies to support preclinical and clinical development of the Lilly portfolio
• Design and implement hypothesis driven studies to answer ADME, PK/PD and clinical pharmacology questions
• Integrate ADME, PK and PK/PD endpoints with discovery biology data to define structure activity- and structure-property-relationships to guide drug delivery and optimization strategies
• Engage, innovate, and collaborate with colleagues and interdisciplinary teams
• Lead the preparation of regulatory communication and documents to support clinical development, new drug applications (NDA and BLA) and line extensions and interact with regulatory agencies worldwide
• Build and foster relationships through coaching and mentorship with fellow scientists
• Possess excellent written and verbal technical communication and the ability to lead, guide and influence teams in decision making

• Experience with PK/PD modeling and/or bio-distribution
• Understanding of and experience with PCR, immunoassay, and/or LC/MS bioanalytical methodology
• Detailed understanding of pharmacokinetics, ADME and proficiency to communicate theory and concepts clearly
• Experience in drug discovery and development
• Ability to balance multiple projects and handle competing responsibilities
• Collaborative team behaviors and aspiration to build and sustain relationships with R&D customers and the wider scientific community
• Experience authoring regulatory and technical reports