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 SUMMARY

As a Research Scientist for our Infusion, Parenteral, and Neurotoxicology (IPN) team located in Senneville, you will be responsible for overseeing study conduct of preclinical efficacy and/or toxicology studies, specifically those with parenteral and CNS routes of administration. Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

• Designs, writes, reviews and edits, as necessary, Study Plans, amendments and study schedules that define and schedule all study activities.
• Oversees and coordinates all aspects of study procedures, whether performed within the department or by service departments.
• Ensures that projects are performed according to Standard Operating Procedures and Good Laboratory Practice regulations and is aware of appropriate regulations, guidelines and guidances.
• Writes, reviews and edits, as necessary, draft or final reports that document all study related procedures and results.
• Prompt verbal or written communication with Sponsors on study related business.

KEY ELEMENTS

We are looking for the following minimum qualifications for this role :

• Bachelor’s degree (BA/BS) or equivalent in Toxicology or related discipline
• Good interpersonal and communication skills;
• Being proficient in English (spoken and written).
• Experience in a GLP environment and/or in preclinical toxicology, an asset
• Strong problem-solving skills.

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;
• Schedule: Weekday schedule, Monday to Friday, 8:30 am to 4:45 pm;
• Permanent position as of the hiring, full time 37.5hrs per week

In this role, primary responsibilities include:

• Designs, writes, reviews and edits, as necessary, Study Plans, amendments and study schedules that define and schedule all study activities.
• Oversees and coordinates all aspects of study procedures, whether performed within the department or by service departments.
• Ensures that projects are performed according to Standard Operating Procedures and Good Laboratory Practice regulations and is aware of appropriate regulations, guidelines and guidances.
• Writes, reviews and edits, as necessary, draft or final reports that document all study related procedures and results.
• Prompt verbal or written communication with Sponsors on study related business

We are looking for the following minimum qualifications for this role :

• Bachelor’s degree (BA/BS) or equivalent in Toxicology or related discipline
• Good interpersonal and communication skills;
• Being proficient in English (spoken and written).
• Experience in a GLP environment and/or in preclinical toxicology, an asset
• Strong problem-solving skills