Job Details

JOB DESCRIPTION

WHY IS THIS A GREAT OPPORTUNITY?

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Montreal, QC rapidly growing GLP preclinical research organization is looking for a seasoned, acknowledged Associate Director, Preclinical Toxicology to advance their already very successful endeavours. They provide preclinical services to the global biotechnology and pharmaceutical industries. The company prides itself on maintaining a family atmosphere and excellent working conditions.

REPORTS TO: Toxicology Director

JOB DESCRIPTION

ROLE AND RESPONSIBILITIES:
- Supervising a number of Study Directors.
- Undertake a SD role as required  re non-clinical safety studies for key clients, large projects, and specialized study types.
- Play a significant role in training of less experienced toxicologists.
-  Advise clients on study design and regulatory issues.
- Take a leading role in in-house committees and task-forces, sales and marketing events.
- Act as Toxicology Director re staff management, special projects, review of study plans and reports.
- Expertise in a specific area of non-clinical safety assessment, as demonstrated by publications (e.g. abstracts, posters,
papers), and/or invited lectures, etc.
- Key person for training of staff, interacting with sponsors, and undertaking management responsibilities.

QUALIFICATIONS

REQUIREMENTS:
Ph.D. in a relevant field, or B.Sc./M.Sc. with DABT Board Certification in Toxicology, or equivalent professional qualification.
5 years' as Senior Toxicologist, Study Director, Senior Research Scientist, or a suitable combination of toxicology -relevant scientific and technical experience.
Small animal R&D, re PK, TK, ADME study experience.
Require deep understanding of toxicology and regulatory issues - PK. TK, related, interpretation of study director reports.
Excellent time management skills and attention to quality.
Must be Canadian citizen or Canadian permanent resident, in Canada or able to return.
 

Education:
University - Bachelor's Degree/3-4 Year Degree