Discovery Toxicology Project Leader

Eli Lilly Eli Lilly · Pharma · Indianapolis, IN

This role leads discovery toxicology project strategy and execution for new pharmaceutical products at Eli Lilly. It involves designing toxicology plans, overseeing studies, analyzing data, and collaborating with cross-functional teams to identify and address toxicity risks for compounds moving into development. The role requires a PhD in Toxicology or related field with relevant experience, strong project management, communication, and data analysis skills, and knowledge of drug discovery, development, and regulatory guidelines.

What you'd actually do

  1. Lead Discovery Toxicology project strategy, and design effective toxicology plans to identify hazards, characterize, and address risk of toxicity for compounds moving into development.
  2. Plan, organize, and oversee Discovery Toxicology studies from initiation to completion, ensuring adherence to deliverables and timelines.
  3. Collect, analyze, and interpret toxicological data, ensuring accuracy and compliance with regulatory standards.
  4. Prepare and present project findings, updates, and reports, to internal and external partners.
  5. Work collaboratively with cross-functional teams to deliver candidates molecules into the development pipeline.

Skills

Required

  • PhD in Toxicology or a related field with 2+ years of relevant experience or MS/BS degree in related field with at least 7 years of applicable experience
  • Discovery or Development Toxicology Project Leader experience
  • Strong communication skills
  • Strong problem-solving skills
  • Strong organizational and project management skills
  • Excellent written and verbal communication skills
  • Proficiency in data analysis and interpretation
  • Knowledge of drug discovery and development process
  • Knowledge of regulatory guidelines and standards (e.g., GLP, FDA, EMA)

What the JD emphasized

  • PhD in Toxicology or a related field with 2+ years of relevant experience or MS/BS degree in related field with at least 7 years of applicable experience.
  • Knowledge of regulatory guidelines and standards (e.g., GLP, FDA, EMA).