Inotiv
Healthcare
ToxicologistII
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Toxicologist II at Inotiv. Skills: Study Director for non-GLP and GLP studies, Manage basic pre-clinical studies, Interpret study data, Prepare final reports. Serve as the Study Director for non-GLP and GLP studies. Prepare study protocols/amendments and assure that protocols and changes are followed.”
What You'll Achieve.
Produce high quality data
Industry & Context.
Assure unforeseen circumstances are noted and appropriate corrective actions are taken and documented.
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 a physical and the use of other PPE (personal protective equipment)
What They're Looking For.
Must Have
M. S. or Ph. D. in toxicology or related field and at least 7 or 3 years experience, respectively., Proficiency in basic computer applications such as email, MS Word and Excel., Effective oral and written communication skills., Able to work independently., 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, 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., 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 a physical and the use of other PPE (personal protective equipment)
Nice to Have
D. A. B. T certification or certification preparation in progress preferred., Previous publications preferred.
What You'll Do.
Serve as the Study Director for non-GLP and GLP studies
Prepare study protocols/amendments and assure that protocols and changes are followed.
Review and approve all study activities
including animal orders
formulation procedures
Observe animals throughout study cycle.
Review study data for scientific quality
and protocol compliance.
Assure unforeseen circumstances are noted and appropriate corrective actions are taken and documented.
Respond to Quality Assurance audits.
Interpret study data and prepare final reports.
Regularly communicate with study Sponsors.
Manages basic pre-clinical studies in accordance with established protocols
and pertinent regulatory requirements.
Reviews training of technical staff to ensure adequacy to perform study-specific techniques.
How You'll Work.
Team & Collaboration
Regularly communicate with study Sponsors.; Serves as a professional resource to other departments.; Ability to accurately interpret and communicate scientific and organizational information with internal and external clients.; Ability to effectively interact with clients.
Communication Scope
Effective oral and written communication skills; Regularly communicate with study Sponsors.; Ability to accurately interpret and communicate scientific and organizational information with internal and external clients.; Ability to effectively interact with clients.
Process & Methodology
Manages basic pre-clinical studies in accordance with established protocols, SOPs, and pertinent regulatory requirements., Responsibility includes conducting several pre-clinical studies concurrently and study complexity may increase with demonstrated competence.
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. * Assure unforeseen circumstances are noted and appropriate corrective actions are taken and documented. * Respond to Quality Assurance audits. * Interpret study data and prepare final reports. * Regularly communicate with study Sponsors. * Manages basic pre-clinical studies in accordance with established protocols, SOPs, and pertinent regulatory requirements. Responsibility includes conducting several pre-clinical studies concurrently and study complexity may increase with demonstrated competence. * Reviews training of technical staff to ensure adequacy to perform study-specific techniques. * Serves as a professional resource to other departments. **_Additional Position Responsibilities_** * May develop and review new proce
Applying for this Toxicologist II role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Workday
- Workday has a multi-step form — save your progress after every section.
- "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
- Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
- Job requisition numbers are useful when following up with HR by email.
ANONYMOUS · UNFILTERED
What do employees actually say about Inotiv?
Real rants from real employees. Read before you apply.