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Lilly Toxicologist-Nonclinical Study Monitor 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.

It is an exciting time to be a part of Team Lilly! Do you have experience working in a GLP environment designing and supervising the conduct of toxicology studies? The Nonclinical Study Management Team (NSMT) is a hardworking and diverse team looking for an experienced Toxicology study monitor with expertise in management of nonclinical safety assessment study conduct, including the fundamentals of Good Laboratory Practices (GLP) and data interpretation of nonclinical studies. We need someone who understands the purpose, components, and outcomes of successful drug development and safety assessment. You will be the primary scientific, technical and procedural contact for studies conducted externally at third party organizations (TPOs). To enable toxicology studies, study managers must understand the technical capabilities of individual TPOs and provide scientific input/expertise on whether studies can be performed as described in the protocol, especially those containing novel procedures.

Responsibilities include establishment of, and adherence to, non-clinical study timelines, monitoring of study conduct at the TPO via communication with the Study Director and/or onsite observation, and real time communication with the Toxicology ADME/ToxPath/Drug Disposition (ATP) team throughout study planning, execution and reporting.

Study Implementation and Conduct:

  • Manage study achievements and metrics to ensure delivery to corporate milestones.

  • The primary Lilly representative that visits TPOs during the course of the study to ensure technical capabilities are adequate and procedures match the protocol.

  • Interact with TPOs as the first line of contact for any study-related issues. Make the initial determination of the impact of the issue on the integrity of the study.

Study Design and Protocol Development:

  • Partner with Toxicology Project Leaders and other scientists to develop study designs and detailed study protocols, including an assessment of the technical ability of the TPO to meet the scientific requirements of the protocol.

  • Resolve any concerns with TPOs regarding specific components of study protocols; whether scientific or logistical.

  • Ensure the protocol meets GLP expectations and protocol-related documentation is available to the TPO prior to study start.

Data Review and Report Writing/Review:

  • Integrate and assemble Toxicology information for IND/CTD and IB documents

  • Serve as point person within Lilly for the receipt, review and interpretation of study data.

  • Coordinate and monitor the internal review of study data to assure compliance with study timelines.

  • Compile all report comments and assure they are conveyed to the Study Director at the TPO

Business Plan Objectives:

  • Lead or collaborate both within department and cross-functionally to accomplish objectives

If this sounds like a match to your skills please apply today. We'd love to have you on our team!

Basic Qualifications:

Bachelor’s degree in Biology, Animal Sciences, Toxicology or a related field with 2 or more years of experience in relevant industry setting

Additional Skills and Preferences:

  • Experience in animal husbandry/in-vivo study conduct within Toxicology

  • Project management experience

  • Excellent communication skills (written and oral)

  • Attention to detail and ability to multitask

  • Good understanding of scientific principles and design of scientific studies

  • Strong teamwork skills with internal and external partners

  • Current understanding of trends of nonclinical safety assessment in the TPO landscape

  • Understanding of Regulatory policies and procedures pertaining to GLP study design and reporting

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 ( LillyRecruitingCompliance@lists.lilly.com ) 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.

Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

As a condition of employment with Eli Lilly and Company in the United States and Puerto Rico, you must be fully COVID-19 vaccinated and provide valid proof of vaccination to the company.

At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people.​ We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!

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