Toxicologist II

Job Title:

Toxicologist II

Qualifications:

M.S. or Ph.D. in toxicology or related field and at least 7- or 3-years' 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.

Corporate Responsibilities:

• Adherence to laboratory health and safety procedures
• Adherence to Standard Operating Procedures (SOPs)
• Adherence to applicable company policies and guidelines
• Adherence to federal and/or local regulations as applicable

Essential Position Responsibilities:

• Serve as the Study Director for non-GLP and GLP studies and performs the following duties for assigned studies:
  • Prepare study protocols/amendments and assure that protocols and changes are followed
  • Review and approve all study activities, including animal orders, formulation procedures, randomization, data collection and timeframes.
  • Observe animals throughout study cycle.
  • Review study data for scientific quality, animal welfare and protocol compliance.
  • Address unforeseen circumstances are noted and appropriate corrective actions are taken and documented.
  • Monitor study costs.
  • Respond to Quality Assurance audits.
  • Interpret study data and prepare final reports.
  • Regularly communicate with study Sponsors.
  • Host client visits.
• Manages complex pre-clinical studies in accordance with established protocols, SOPs, GLPs, and other pertinent regulatory requirements. Responsibility includes conducting multiple pre-clinical studies concurrently.
• Reviews training of technical staff to ensure adequacy to perform study specific techniques.
• Reviews and develops new procedures, technologies, and SOPs as required.
• Serves as a professional resource to other departments.

Additional Position Responsibilities

• Prepares manuscripts and/or presents at scientific meetings.
• Other duties as assigned.

Additional 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 while working under the pressure of strict deadlines.
• Weekend and holiday work as required.
• Work requires entrance into the Vivarium areas. Demonstrated immunological tolerance as necessary to be present in animal areas.
• Work requires passing annual physical and the use of other PPE (personal protective equipment)

Professional Responsibilities: (if applicable)

• Attends continuing education courses, as appropriate.
• Maintain an active involvement in professional organizations.
• Be knowledgeable in regulatory requirements.

The annual pay range estimated for this position is $80,100 to $105,500. Please note that salaries vary within the range based on factors including, but not limited to, prior relevant experience, skills, education, certification, location as well as internal equity and market data.

*This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience. The salary range will adjust along with the level of the role to match the person's relevant experience and/or education level.

At Inotiv, our work helps advance the development of new medicines and therapies that can improve people's lives. As a leading global contract research organization (CRO), we partner with researchers to tackle complex scientific challenges, drive innovation, and help build a healthier, safer world. Bringing together scientists, researchers, technical experts, and business professionals, we provide the expertise and collaboration needed to move research forward. Our people make this work possible, and we value the knowledge, ideas, and contributions each person brings to the team. Whether you are starting your career or bringing years of experience, Inotiv offers opportunities to learn, grow, and play a meaningful role in advancing treatments for patients around 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.