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.

KEY ELEMENTS

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

• Student for bachelor’s degree in pharmacology, immunology, biochemistry, biomedical sciences, Toxicology, or equivalent fields, preferably in the last year of the program.
• Experience in scientific data presentation, writing, editing, and proofreading preferred.
• Ability to work autonomously and very organized;
• Able to work under time constraints and possess the ability to deal with a variety of pressing issues on a regular basis in a rapidly changing environment.
• Bilingualism is required.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

ROLE SPECIFIC INFORMATION:

• Location: 1580 rue Ida-Métivier, Sherbrooke (Fleurimont), QC, J1E 0B5
• Transportation: Easily accessible using Sherbrooke’s public transit system. Free parking. Electric vehicle charging station
• Salary: Starting at $20.00/hr, to be discuss.
• Schedule: Daytime between Monday to Friday. Depending on the needs and deadlines to be respected, you may have to do overtime.
• Temporary position, full-time 37.5hrs per week;

In this role, primary responsibilities include:

• Lead the scheduling and reporting process for a number of studies by providing support to the assigned Study Directors;
• Autonomously manages the receipt, distribution, pursue of, and address of study plan and report comments with scientific judgment and accuracy;
• Coordinate and collaborate with involved departments and external contributors to produce quality, on-time Study Plan and reports;
• Ensure availability/completion of all required documents and notifications in support of study conduct and report finalizations;
• Communicate effectively and own the ability to adhere to timelines, and providing support to the assigned Study Director(s) when reporting timelines require changes/updates

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

• Student for bachelor’s degree in pharmacology, immunology, biochemistry, biomedical sciences, Toxicology, or equivalent fields, preferably in the last year of the program.
• Experience in scientific data presentation, writing, editing, and proofreading preferred.
• Ability to work autonomously and very organized;
• Able to work under time constraints and possess the ability to deal with a variety of pressing issues on a regular basis in a rapidly changing environment.
• Bilingualism is required