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MPI Research: Study Director – Safety Pharmacology

MPI Research

This is a Full-time position in Montreal, QC posted June 6, 2021.

Job Summary We are seeking a Study Director for our Safety Pharmacology department site located in Laval (Greater Montreal area) in Canada.

This person will undertake the role of Study Director for the conduct of non-clinical safety (Toxicology, Safety pharmacology, Toxico/Pharmacokinetics) studies in animals.

Long Description Responsabilities : Develop and approve study plans in consultation with Scientists and sponsors, ensuring that the studies are planned efficiently with regards to the number of animals required, staff requirements and qualifications, animal welfare issues and health and safety legislation; Ensure that studies areconducted in accordance with the study plan, Standard Operating Procedures (SOPs) ; Ascertain availabilitiyof test substance prior to commencement of study and throughout its duration; Ensure that study personnel are fully aware of their required duties within the studies, including data collection and integrity.

Monitor the test system during the study by conducting a minimum of weekly visits to the animals room, by supervising critical activities and reviewing the records as appropriate; Perform appropriate analysis and interpretation of study data generated by Clinical Pathology and Toxicology departments; Integrate the various elements of data analysis and their interpretation provided by the contributing scientists on the study; Communicate appropriateinformation concerning studies to the sponsor, management, study management team, Quality Assurance Program, so that appropriate decisions and actions are carried out; Respond promptly to QAPinspection finding; Ensure the production of study reports are on time by signing the report confirming that he is familiar and in agreement with the study findings, their interpretations and the evidence that support the interpretations based on available data.

Job Qualifications Bachelors degree in a scientific field or equivalent; 1 to 2 years experienceas Scientist I or in a suitable combination of relevant scientific and technical experience in toxicology; Good practical experience in project management; Good knowledge of related legislation, principles, practices and procedures; Good knowledge and application of Good Laboratory Practices (GLP); Communication (written and spoken) in English is essential.

Bilingualism is preferable; Strong organizational, interpersonal and communication skills; Strong problem-solving and analytical skills; Ability to work under time constraints and adapt to change; Strong customer serviceorientation; Meticulous attention todetail; Working knowledge of related computer applications