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Principal Study Director/Toxicology
Tech USA 57 reviews Rockville, MD Get job updates from Tech
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Qualifications: **
M.S. or Ph.D. in toxicology or related field and at least 2 years About this company
experience preferred. D.A.B.T certification or certification
preparation in progress preferred. Additional experience may Tech USA
substitute for educational requirements. 57 reviews
Proficiency in basic computer applications such as email, MS Word TechUSA is a nationwide staffing solutions
and Excel. agency that provides customized staffing
Effective oral and written communication skills. and consulting support to both government
Previous publications preferred and commercial...
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: **
Perform Study Director responsibilities 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 preclinical studies in accordance with
established protocols, SOPs, GLPs, and other pertinent
regulatory requirements. Responsibility includes conducting
multiple preclinical studies concurrently.
Reviews training of technical staff to ensure adequacy to
perform study specific techniques.
Assists business development in the preparation of
proposals.
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 multitask and participate in multiple preclinical
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
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4/25/2016 Principal Study Director/Toxicology job - Tech USA - Rockville, MD | Indeed.com
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.**
Job Type: Fulltime
Required experience:
Toxicology or related field: 2 years
Required license or certification:
D.A.B.T certification or certification preparation in progress
preferred
Required education:
Master's
12 days ago
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