Lilly ADME Project Leader – Innovation Solutions in Indianapolis, Indiana
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.
Since 2014, Lilly has launched 18 new molecular entities globally, with several high value launches yet to come. Looking ahead, we have a new challenge: to sustain this productivity and drive additional growth. To push to this next level, Lilly is building a new model that allows us to participate in and advance external biotechnology innovation.
We see an opportunity for Lilly to provide value-added R&D solutions including discovery and development capabilities and consultation to drive external innovation. Ultimately, we envision a R&D solutions business that engages with hundreds of companies around the world, providing a superior partnering experience vs. CROs, and creating a shared interest in their success.
In support of this new model, the ADME/Toxicology/PKPD (ATP) organization is seeking an experienced drug discovery and development ADME scientist interested in leveraging their expertise to bring the needed capabilities to each new external partnership. You will work with a team of like-minded scientists to provide expertise in areas including toxicology, pathology, drug metabolism, pharmacokinetics/bioanalytical, translational/predictive drug disposition, PKPD, and immunogenicity across multiple modalities to advance various external innovation initiatives. You will engage in consultation, experimental design, execution and/or data interpretation to help deliver a diverse external portfolio of investigational targets and novel therapeutics.
If you are interested in applying your expertise to advance the science of drug discovery and development working in a highly collaborative, innovative setting, we hope you’ll consider joining us.
Engage in ATP-focused discussions as an advisor/consultant with external start-up and biotechnology companies to develop testing strategy to achieve drug discovery and development milestones
Provide ADME expertise to shape study designs, aid issue resolution, and interpret data
Leverage ATP experts to navigate internal vs. external work plans
Prepare nonclinical data packages to support global regulatory submissions and correspondence; engage with global regulators
Partner with R&D Solutions ATP leader to forecast capability demand, strategy for internal vs. external work execution, and build a suite of ATP capabilities to offer external companies.
Thorough understanding of first-principles in biopharmaceutics, drug absorption, metabolism, transport, clearance, and pharmacokinetics, along with an ability to clearly communicate theories and concepts
Strong understanding of global regulatory guidances that shape the ADME program strategy
Experience leading drug discovery and development programs as the ADME expert through significant milestones (candidate identification, first-in-man studies, proof-of-concept).
Collaborative team behaviors and desire to build and sustain relationships with R&D colleagues, external partners, and the wider scientific community
Strong passion for pharmaceutical innovation
Adept at working with cross-functional colleagues
Excellent self-management and organizational skills
Demonstrated strong collaboration and communication skills
Familiarity with business development, such as search and evaluate, due diligence, or transactions, or experience working with external partners, including start-up and biotechnology companies
Ph.D. degree in Drug Metabolism, Pharmacokinetics, or Pharmaceutics, Chemistry, or an advanced degree in a related science with extensive relevant training
Minimum 10 years of experience in the pharmaceutical industry including significant experience in drug discovery and development in one of the above scientific disciplines
Experience in drug discovery and development across multiple modalities and therapeutic areas
Ability to handle multiple simultaneous projects and manage competing priorities
- Some travel required for conferences and external company meetings
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Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.
As a condition of employment with Eli Lilly and Company and its subsidiaries in the United States and Puerto Rico, you must be fully COVID-19 vaccinated and provide proof of vaccination satisfactory to the company (subject to applicable law).