| Job #: | 357 |
|---|---|
| Title: | Preclinical Toxicology Study Director |
| Job Location: | Montréal, Quebec - Canada |
| Employment Type: | Full Time / Direct Hire |
| Salary: | contact recruiter for details |
| Other Compensation: | benefits |
| Employer Will Recruit From: |
Local
Quebec Province |
| Relocation Paid?: | NO |
Excellent preclinical toxicology study director position with rapidly growing company - animal studies, necropsies, ADME, PK, GLP
Montreal, QC preclinical testing laboratory seeks a Toxicology Study Director to be responsible for toxicological (GLP) investigation of pharmaceuticals.
ROLE AND RESPONSIBILITIES:
Designing protocols and programs.
Overseeing all technical and scientific activities and in-life monitoring.
Communicating with sponsors.
Writing reports and evaluating data.
Serving as the scientific representative on corporate committees.
Attending scientific meetings.
Training of junior technical and scientific personnel.
Carry out R&D in line with company objectives.
REQUIREMENTS:
B.Sc.. (min) plus 5 years as a Toxicology Study Director in the CRO, biotechnology, OR pharmaceutical industry.
Experience with safety studies of biologics and drugs.
Excellent organizational and report writing skills, working knowledge of GLP.
French / English bilingual preferred.
Education:
University - Bachelor's Degree/3-4 Year Degree
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