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. Addi…
Skills: Toxicology, Study direction, GLP compliance, Protocol development, Data analysis
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$80k–$106k/yr
Full-time
postgraduate degree
Health coverage, Dental coverage, Short-term disability, Long-term disability, Paid time off, Paid parental leave
Posted 25d ago
~40 hrs/week
Responsibilities
The Toxicologist II serves as a Study Director for non-GLP and GLP studies, overseeing study protocols, animal welfare, and data quality. They are responsible for managing complex pre-clinical studies, interpreting data, and communicating findings to sponsors and regulatory bodies.
Requirements
Candidates must hold an M.S. or Ph.D. in toxicology or a related field with relevant professional experience. Proficiency in computer applications, strong communication skills, and the ability to work in a laboratory/vivarium environment are required.
Full job description
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.
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.
WHERE INSIGHTS LEAD TO ANSWERS
Expect More
In choosing a partner for discovery, development and research models, expect more: more attention, more insight, and a superlative experience. You’ve worked hard to get this far, and you deserve a provider seamlessly aligned to your needs and goals.
Through scientific leadership and ongoing investments, Inotiv delivers a comprehensive range of services and products that will exceed your expectations. Benefit from our long and impeccable regulatory history, world class team of scientists, and track record of providing attentive, decisive service.
Answering the right questions on time and with high-quality data is the key to achieving your objectives. At Inotiv, that is our focus: to provide you with both the broad scope and right-size solutions essential to your success.
Gain the insights you deserve to get the answers you need. Expect more — with Inotiv.
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Offices: 2701 Kent Ave., West Lafayette, IN 47906, US