Due to business expansion, we are looking to fill several new positions, we are looking for candidates who shares our passion for science and research. Our mission is to bring new medicines into the world to improve the quality of life and prolong the life expectancy of people. Be part of this dynamic team and start changing the lives of people!.
• Design and prepare study plans, amendments and reports;
• Prepare and/or review study-related documentation;
• Ensure all documentation associated with studies is up-to-date and complies with
Study Plan, departmental and company Standards Operational Procedures (SOPs);
• Coordinates study related activities where necessary with the section leaders;
• Instructs and liaises with inhalation technicians in generation and sampling procedures and technical work;
• Interprets and reports study data generated from all departments involved on a study;
• Liaises with Sponsors, consultants and Principal Investigators on study-related matters;
• Participates in client visits relating to studies assigned to them;
• Substitute for and/or assist other study directors if needed;
• Be conversant, and function in compliance with guidelines and regulations published by governmental regulatory bodies (OECD, FDA, EPA and HPB). Participates in the review and revision of SOPs;
• Remain informed on technology developments by self-education and/or external
trainings, as required;
• Participates in Toxicology meetings;
• Assists in maintaining a safe working environment for himself/herself and his/her colleagues by observing all safety procedures and working methods;
• Performs other related duties;
• B.Sc. or M.Sc. in a science related field with a preference to biology based;
• A minimum of three years of experience in a related field;
• Good knowledge of GLP;
• Excellent problem solving and analytical skills;
• Ability to work under time constraints and to adapt to change.
• Experience working with laboratory rodents and large animal species’
• Proficient in English (spoken and written) and able to communicate in French;
• Good report writing abilities;
• Autonomous, organized with the ability to lead;
Conditions: Permanent, day-time, full-time (37.5 hr./week)
To apply: Please send your CV and a cover letter to: abitar@itrlab.com
Deadline: ASAP
Fields marked with an asterisk (*) are required.
