Research associate - Toxicology - Jobs in Senneville, QC

Job Description

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe.IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly.Job SummaryThe research associate is responsible to coordinate and plan the study related activities according to the study plan and SOP. He is a resource for the study director and the technical team. As a team, they have to coordinate with different groups to carry out the studies successfully. They have to be flexible with the nature of the work. The research associates are the central communication point from the start to the end of the study.Long term planningForecast the workload using the tools at their disposition.Pre study planningReview the study plans and discuss the specific needs for the study with the scientific staff.Prepare the study schedule and ensure the material is available and/or ordered.Prepare the needs to cover the activities and forward them to the scheduler.Coordinate the study activities with the other departmentsMonitoring in lifeCoordinate last minute activities/changes with the team leader, study director and the other departments.Ensure the forms used are appropriate for data collection.Follow the health status of the animals and inform the study director and team leader of any health changes or issuesRevisionReview of data collected and write the deviations related to the data reviewed.Job QualificationsEducation: DEC Preferred (DEC in Animal Health, asset)Experience : 5 to 6 yearsAn equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.ADVANTAGES :On the job training;Possibility of internal advancement according to strengths and interests;Competitive benefits - Dental, Drug, Physiotherapy, Psychotherapy, Optometrist, Life Insurance, RRSP/TFSA participation;Uniform provided;Free parkingIMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.About Safety AssessmentCharles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.Quick Apply

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