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. As a leading contract research organization (CRO), Inotiv supports discovery and nonclinical development through investigational new drug (IND) and beyond. By leveraging our deep expertise and scientific capabilities, we help you increase efficiency, improve data, and reduce the cost of taking new drugs to market. By providing critical research models and related services, we help researchers realize the full potential of their R&D projects, all while working together to build a healthier and safer world. We hope you consider our opportunities and a future with Inotiv!

Requirements

  • M.S. in physical/life science
  • PhD. In physical/life science
  • 7+ years’ experience in scientific research/testing (preferably toxicology)
  • 5+ years’ experience in scientific research/testing (preferably toxicology)
  • Expertise in analyzing, manipulating, and interpreting large toxicological data sets from in vitro, in vivo, and in silico toxicology studies utilizing computational methods to analyze, simulate, visualize, characterize and/or predict the toxicity of chemicals; experience with PBPK and/or IVIVE is extremely helpful
  • Excellent communication skills including strong, proven technical writing and editing skills
  • Excellent laboratory skills
  • Excellent organizational skills
  • Ability to exercise independent judgment
  • Function well independently or in a team environment
  • Computer skills with Windows/Mac OS, MS Word/Excel/Outlook, and proficiency with R or Python

Responsibilities

  • Develop approaches to analyze the pharmacokinetic behavior of chemicals (PBPK, IVIVE)
  • Oversight of laboratory operations for RNAseq and Error-corrected sequencing, including study design, ordering, conduct of experiments
  • Generate, analyze and report performance of test chemicals in in silico and in vitro test systems
  • Consultation on experimental design and statistical analyses
  • Providing scientific expertise at meetings (internally, at public forums/workshops, and conferences)
  • Developing, writing, reviewing scientific documents, publications, and presentations
  • Preparing graphical presentations using appropriate computer programs
  • Providing scientific leadership
  • Contribute to proposals and business development
  • Participate in client calls
  • Document workflows rigorously
  • Contribute to thought leadership (white papers, webinars, conference talks)
  • 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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