Toxicologist - Study Monitor at Lilly

Indianapolis, Indiana, United States -

Full Time

Start Date

Immediate

Expiry Date

02 Jan, 26

Salary

169400.0

Posted On

04 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Toxicology, Good Laboratory Practices, Project Management, Communication Skills, Attention to Detail, Multitasking, Scientific Principles, Teamwork, Animal Husbandry, Data Interpretation, Study Design, Protocol Development, Regulatory Policies, Study Monitoring, Study Reporting, Technical Capabilities

Industry

Pharmaceutical Manufacturing

Description

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. 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 39,000 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. #WeAreLilly 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 toxicology 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 Basic qualifications: Bachelor’s degree in Biology, Animal Sciences, Toxicology or a related field with 3 or more years of experience in relevant industry setting Additional Skills and Preferences: Experience in animal husbandry/invivo 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 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. Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities participate in the workforce and ensure equal opportunity to compete for jobs. If you are an individual with a disability and require a reasonable accommodation to participate in the application process, please email Lilly Recruiting Compliance. Please note, this email address is intended for use only to request a disability accommodation, please email Lilly Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $65,250 - $169,400 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

Responsibilities

The Toxicologist - Study Monitor will manage the conduct of toxicology studies at third-party organizations, ensuring adherence to protocols and GLP standards. Responsibilities include monitoring study progress, resolving issues, and collaborating on study design and data interpretation.