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(816) 333-9772
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Director, Toxicology
Will plan and manage pre-clinical toxicology studies. Act as a hands-on Senior Study
Director, managing studies and providing leadership and guidance for a team of toxicology
study specialists. Will be a technical
expert and resource for the company. Specific individual and management duties include:
* Overall study oversight and management
including technical conduct of the study, interpretation, documentation and reporting of
results.
* Primary point of contact with Sponsor
on all study related issues.
* Prepare study protocols and amendments, obtain appropriate signatures, arrange for
distribution and QA audit, if required.
* Submit IACUC review form.
* Arrange for the required amount of test articles to be delivered.
* In accordance with the SOPs, review and approve study events, i.e.,
animal orders, formulation procedures, randomization, and any
specialized data collection forms.
* Arrange and conduct study pre-initiation meeting.
* Periodically observe animals, critical phases and review study data
for scientific quality, animal welfare and compliance with protocol,
SOPs and applicable regulations.
* Monitor study budget and time line.
* Respond to QA audits
* Oversee reporting writing process including writing summary, results,
and conclusions, reviewing drafts, receiving and addressing client
comments, interacting with contributing scientists as necessary, and
approving the final report.
Requirements
Requirements:
* PhD, DABT desired (or working toward certification) with at least 7
years of toxicology experience.
* Expertise in toxicology, reproductive toxicology (DART), immunology,
pharmacology and/or related fields.
* Supervisory experience
* Good problem-solving skills.
* Excellent computer, communication and writing skills. |
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To express your interest in this
position,
visit our Applicants page
to fill out the short registration form
or
E-mail Harlan Staffing Consultants. |
