Job OverviewResearch Scientist II - InhalatonAs a
Research Scientist II for our
Inhalation team at the
Senneville location, you will be responsible for planning, coordinating, and overseeing study activities to ensure compliance with regulatory standards and high-quality scientific outcomes.
In this role, primary
responsibilities include:
- Execute and manage studies of moderate to high complexity;
- Design, write, review, and edit study plans, amendments, and study schedules to effectively define and organize all study-related activities;
- Oversee and coordinate all aspects of study procedures, whether conducted within the department or in collaboration with external service groups;
- Monitor project scope, staffing, and equipment needs; communicate effectively with leadership on resource planning;
- Support proposal development and project management under supervision;
- Participate in the design, development, and implementation of new procedures;
- Prepare scientific abstracts and present research findings internally and externally as appropriate;
- Act as a departmental representative in cross-functional initiatives and communications;
- Prepare, review, and finalize draft and final reports documenting all study procedures, data, and results in a clear and accurate manner;
- Host client visits, lead or support facility tours, and participate in client meetings (telephone/video conferences);
- Mentor junior staff and support training of research scientists;
- Ensure all projects are executed in accordance with Standard Operating Procedures (SOPs) and Good Laboratory Practice (GLP) regulations, while maintaining up-to-date knowledge of relevant regulatory guidelines.
Key ElementsWe are looking for the following
minimum qualifications for this role:
- Minimum of a bachelor's degree (BA/BSc) in toxicology, pharmacology, or a related discipline.
- Minimum of 5 years' related experience in the research industry.
- Proven ability to oversee and coordinate study conduct, including protocol development, technical guidance, and reporting
- Strong understanding of the full study lifecycle, from proposal development through to final report completion
- Demonstrated experience designing and reviewing study plans, amendments, and study schedules
- Experience writing, reviewing, and editing draft and final reports that accurately document study procedures and results
- Excellent attention to detail with strong scientific writing and organizational skills.
- Excellent project management and organizational abilities
- In-depth knowledge of GLP and regulatory requirements
- Ability to coordinate cross-functional teams and manage multiple priorities
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, John Abbott College and from the REM station of l'Anse à l'Orme to the Senneville site. Free parking. Electric vehicle charging station;
- Annual bonus based on performance;
- Schedule: Monday-Friday, Day schedule with 6 weekends per year;
- Permanent position as of the hiring, full-time 37.5hrs per week.
- Salary: The hiring range for this position is $73,000 to $99,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications and location
Why Charles River ? - We offer competitive benefits and advantages from day one to support your well-being;
- 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);
- 4 weeks' Vacation & 10 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.
