Due to our continued growth, ITR Laboratories Canada, Inc. is looking for experienced toxicologists to act as Study Directors overseeing the conduct of GLP-compliant toxicology studies of pharmaceuticals. Motivated candidates, fluent in English (French an asset) with an education and / or experience in pre-clinical research are invited to apply.
Responsibilities of the position include program / protocol design and preparation, direction /oversight of all scientific & technical activities, in-life monitoring, Sponsor communications, data evaluation and report writing. The selected candidate(s) will also act as scientific representative on internal committees, represent the company at scientific meetings, train junior scientific and technical staff, and direct/execute research and development strategies consistent with company objectives.
QUALIFICATIONS: Minimum of a BSc. with 5 years in the pharmaceutical, biotechnology or CRO industry as a Study Director.
SKILLS: Study Director, experience with safety studies of drugs & biologics; well-developed organizational and communication (written and verbal) skills; superior report writing abilities; thorough knowledge of GLP.
Remuneration will be commensurate with qualifications and experience. We offer a relocation package for overseas applicants. Interested parties should submit their resumes to:
ITR Laboratories Canada Inc.
Fax: (514) 457-8784
E-mail: hr@itrlab.com
