Director - Veterinary Clinical Pathologist
Eli Lilly and Company
4 hours ago
On-site
Indianapolis, IN
$169,500 - $312,400 USD yearly
Operations
Eli Lilly & Company is seeking a versatile and energetic veterinary clinical pathologist to work in drug discovery and development at the Lilly Corporate Center in Indianapolis, IN.
Responsibilities:
- Provide scientific leadership in interpreting toxicity and pharmacologic effects caused by biopharmaceuticals
- Design, conduct, interpret, and peer review clinical pathology-related endpoints in animal studies supporting drug development (including pharmacology and toxicology studies)
- Identify and bring solutions to pathology and toxicology issues affecting discovery and development of potential biopharmaceuticals
- Collaborate with a team of anatomic pathologists, toxicologists, nonclinical study managers, and other scientists
- Interact frequently with external business partners (assessing laboratory capabilities, validating assays, supporting biomarker development and/or outsourcing, and peer reviewing study results)
- Partner with scientists using translational and comparative medicine expertise to positively impact Lilly’s projects
Basic Qualifications:
- DVM or equivalent degree and certification by the American College of Veterinary Pathologists (Clinical Pathology)
- Minimum of 7 years of experience evaluating, interpreting, and reporting GLP and non-GLP clinical pathology data from nonclinical toxicity studies
Additional Skills/Preferences:
- Experience integrating clinical and anatomic pathology data from nonclinical toxicity studies
- Experience evaluating and reporting pathology data from animal models of human disease or other drug discovery studies
- Clear, concise oral and written communication of pathology data
- Ability to work independently and in cross-functional teams on drug discovery and development issues
- Ability to develop scientific/regulatory perspectives on emerging issues; strong problem-solving skills
- Experience with multiple therapeutic modalities
- Training or certification in anatomic pathology
- Ability to travel to business partners and regulatory agencies
- Familiarity with biomarker development practices, designing validation studies, and authoring reports
Benefits:
- Eligibility for company bonus (depending, in part, on company and individual performance)
- Comprehensive benefits program for eligible employees (e.g., 401(k), pension, vacation, medical/dental/vision/prescription, flexible benefits, life insurance, certain time off/leave, and well-being benefits)
Compensation:
- Anticipated wage: $169,500 - $312,400
Application Instructions:
- If you require accommodation to submit a resume, complete the accommodation request form: https://careers.lilly.com/us/en/workplace-accommodation
Responsibilities:
- Provide scientific leadership in interpreting toxicity and pharmacologic effects caused by biopharmaceuticals
- Design, conduct, interpret, and peer review clinical pathology-related endpoints in animal studies supporting drug development (including pharmacology and toxicology studies)
- Identify and bring solutions to pathology and toxicology issues affecting discovery and development of potential biopharmaceuticals
- Collaborate with a team of anatomic pathologists, toxicologists, nonclinical study managers, and other scientists
- Interact frequently with external business partners (assessing laboratory capabilities, validating assays, supporting biomarker development and/or outsourcing, and peer reviewing study results)
- Partner with scientists using translational and comparative medicine expertise to positively impact Lilly’s projects
Basic Qualifications:
- DVM or equivalent degree and certification by the American College of Veterinary Pathologists (Clinical Pathology)
- Minimum of 7 years of experience evaluating, interpreting, and reporting GLP and non-GLP clinical pathology data from nonclinical toxicity studies
Additional Skills/Preferences:
- Experience integrating clinical and anatomic pathology data from nonclinical toxicity studies
- Experience evaluating and reporting pathology data from animal models of human disease or other drug discovery studies
- Clear, concise oral and written communication of pathology data
- Ability to work independently and in cross-functional teams on drug discovery and development issues
- Ability to develop scientific/regulatory perspectives on emerging issues; strong problem-solving skills
- Experience with multiple therapeutic modalities
- Training or certification in anatomic pathology
- Ability to travel to business partners and regulatory agencies
- Familiarity with biomarker development practices, designing validation studies, and authoring reports
Benefits:
- Eligibility for company bonus (depending, in part, on company and individual performance)
- Comprehensive benefits program for eligible employees (e.g., 401(k), pension, vacation, medical/dental/vision/prescription, flexible benefits, life insurance, certain time off/leave, and well-being benefits)
Compensation:
- Anticipated wage: $169,500 - $312,400
Application Instructions:
- If you require accommodation to submit a resume, complete the accommodation request form: https://careers.lilly.com/us/en/workplace-accommodation