For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well:being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about. Job Summary As a Study Coordinator for our Study Coordination Support team located at theSenneville site, you will assist the Scientist during in:life and reporting by providing and/or coordinating scientific, administrative and project planning support for basic to moderate complex study designs, to ensure the production of a high quality and timely study report. In this role, primary responsibilities include: :Schedule and monitor study milestones using appropriate software application (RPM, Front End and CID). :Monitor events during the in:life phase by reviewing study related documents (study plans/amendments) upon issuance to assure full understanding of assigned projects in order to assess impact on timelines and reporting requirements. :Other individual tasks as delegated by Supervisor to ensure departmental workflow :Perform all other related duties as assigned. Key Elements We are looking for the following minimum qualifications for this role: :DEC ; :Comfortable following procedures; :Comfortable working on a computer; :Motivated, autonomous, and meticulous person; :Positive attitude and good team spirit. Role Specific Information: :Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1; :Transportation: We offer a free shuttle service from the Sainte:Anne:de:Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station; :Salary: 26/hour; :Annual bonus based on performance; :Schedule:Monday to Friday from 8am to 4:15pm :Permanent position as of the hiring, full:time 37.5hrs per week. Why Charles River ? :Competitive benefits as of the hiring. We pay up to 85 of premiums (health and dental coverage); :Free gym on site; :Employee and family assistance program; :Excellent welcome program for new employees as well as in:house advancement and career development opportunities; :Access to a doctor and various health professionals (telemedicine); :3 weeks' Vacation and 5 Personal day policy; :Many social activities If you are interested in contributing to the well:being of our communities, not only across the country but around the world, please join us. This is Your Moment. About Safety Assessment Charles 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 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities. About Charles River Charles River is an early:stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non:GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model