Toxicologist II

Inotiv is a growing contemporary drug discovery and development company focused on delivering world-class solutions that impact global health and well-being.

Qualifications

• M.S. or Ph.D. in toxicology or related field with at least 7 or 3 years of experience, respectively
• D.A.B.T certification or certification preparation in progress preferred
• Additional experience may substitute for educational requirements
• Proficiency in basic computer applications such as email, MS Word, and Excel
• Effective oral and written communication skills
• Previous publications preferred
• Able to work independently
• Demonstrated immunological tolerance to work in Vivarium areas
• Ability to pass annual physical and use personal protective equipment (PPE)

Responsibilities

• Serve as the Study Director for non-GLP and GLP studies, including:
  • Preparing study protocols/amendments and ensuring compliance
  • Reviewing and approving study activities (animal orders, formulation procedures, randomization, data collection, and timeframes)
  • Observing animals throughout the study cycle
  • Reviewing study data for scientific quality, animal welfare, and protocol compliance
  • Addressing unforeseen circumstances, documenting corrective actions
  • Monitoring study costs and responding to Quality Assurance audits
  • Interpreting study data and preparing final reports
  • Regularly communicating with study Sponsors and hosting client visits
• Manage complex pre-clinical studies in accordance with established protocols, SOPs, GLPs, and regulatory requirements, including conducting multiple studies concurrently
• Review training of technical staff to ensure adequacy for study-specific techniques
• Review and develop new procedures, technologies, and SOPs as required
• Serve as a professional resource to other departments
• Prepare manuscripts and/or present at scientific meetings
• Adhere to laboratory health and safety procedures, SOPs, company policies, and federal/local regulations
• Perform other duties as assigned

Requirements

• Ability to multi-task and participate in multiple pre-clinical research studies concurrently
• Ability to accurately interpret and communicate scientific and organizational information with internal and external clients
• Ability to effectively interact with clients and regulatory personnel
• Ability to produce high-quality data under strict deadlines
• Weekend and holiday work as required
• Maintain involvement in professional organizations and continuing education
• Be knowledgeable in regulatory requirements

Pay

The annual pay range for this position is $80,100 to $105,500, varying based on prior relevant experience, skills, education, certification, location, internal equity, and market data. The position may be offered at different levels depending on the candidate’s qualifications.

Benefits

• Health and dental coverage
• Short- and long-term disability
• Paid time off
• Paid parental leave
• 401K and more