Toxicologist II

InotivKeystone, NC
15h$80,100 - $105,000Remote

About The Position

Inotiv is a growing contemporary drug discovery and development company where we “Play to Win” in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world. There’s an opportunity for everyone at all phases of a career, each individual’s unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people’s lives, we have the career opportunities to make it happen. Join us in embracing research and science to impact the health and well-being of people all over the world. Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more! Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.

Requirements

  • M.S. in physical/life science
  • Ph.D. in physical/life science
  • >10 years of professional experience
  • >7 years of professional experience
  • Toxicology (Board certified preferred)
  • Strong technical writing and organizational skills
  • Ability to exercise independent judgment, multi-task, and meet short-term deadlines
  • Function well independently and in a team environment
  • Excellent communication skills

Responsibilities

  • Review and prioritize searches
  • Prepare report outlines
  • Write sections of Report on Carcinogens (RoC) monographs
  • Write summary profiles for chemicals or other substances listed in the RoC
  • Prepare SOPs and protocols
  • Review and edit project deliverables
  • Develop and maintain database(s) for animal studies
  • Review and edit work prepared by outside consultants and coordinates activities of project staff to meet deliverable deadlines.
  • Review, edit and summarize mechanistic and animal data in published literature.
  • Work in a team environment with a professional and positive attitude
  • Other duties as needed

Benefits

  • health and dental coverage
  • short- and long-term disability
  • paid time off
  • paid parental leave
  • 401K
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