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 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.
The Nonclinical Safety Assessment group is seeking a Toxicology Project Leader to join our team. The successful candidate will provide scientific leadership and drug development expertise. They will represent Toxicology on drug development teams from early discovery through clinical trials to registration and beyond. This role is crucial in developing world-class medicines for Eli Lilly and Company. It also offers leadership and advancement opportunities within the Division of Toxicology/Pathology, a multidisciplinary group dedicated to predicting and evaluating the safety of novel drug candidates.
Are you interested in working on life changing medicines? Apply today to help bring life-changing therapies to patients at Lilly. We need to you as we continue to expand our portfolio to drive effective solutions for patients.
Responsibilities:- Toxicology representative on diverse scientific teams, working collaboratively across multiple functions including Chemistry, Discovery Biology, Drug Disposition, Pathology, Medical/Clinical, and Regulatory Affairs within Lilly and with external research organizations
- Lead toxicology strategy, and design effective toxicology plans to identify issues, characterize, and address risk of toxicity for compounds moving through development.
- High level of impact both internally within Lilly and in the external research and/or regulatory environment.
- Contribute to a group of highly engaged scientists, providing industry-leading toxicology support to development teams.
Basic Qualifications:- PhD in Toxicology or a related field with 5+ years of relevant experience or MS degree with at least 10 years of applicable experience post education or training
Additional Skills/Preferences:- Experience developing and coordinating nonclinical development strategies for various stages of pharmaceutical development and preparing a nonclinical safety assessment for clinicians and regulatory agencies.
- Knowledge of global regulatory guidance (e.g. ICH and geography-specific guidance's) and Good Laboratory Practice (GLP) standards
- Diplomate, American Board of Toxicology (DABT)
- Strong verbal and written communication skills
- Ability to work effectively in a team environment
- Experience/expertise with development of novel modalities highly valued
- Role is located at the Lilly Corporate Center in Indianapolis, IN
Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively "Lilly") are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.
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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.