Inotiv
Healthcare
ToxicologistII
“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.
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