Research Scientist Job at Charles River Laboratories
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 a Non-Clinical Studies Manager for the General Toxicology Department located in Sherbrooke, it is mainly a face-to-face position.
In this role, key responsibilities may include:
- Designs, writes, reviews and edits study plans, amendments and study schedules that define and schedule all study activities.
- Works on studies/programs of basic to moderate complexity.
- Supervises and coordinates all aspects of study procedures, whether performed within the department or by service departments.
- Communicate effectively with Sponsor and internally to build trust
- Advises the Sponsor and advises the technical teams on the experimental design or during the conduct of the study.
- Ensures that projects are carried out in accordance with standard operating procedures and rules of good laboratory practice and knows the appropriate regulations, directives and guidelines.
- Write, review and revise, if necessary, draft reports or final reports that document all procedures and results related to the study.
- Communicate promptly, orally or in writing, with sponsors on study-related matters
- Be the sole point of control for decisions related to the studies assigned, and in this sense, be very available.
- Have a sense of reprioritization according to needs and be able to work in a dynamic and rapidly changing environment.
Key Elements
If you possess the following qualitifications, we will train you in the rest:
- Education: Minimum of a Bachelor's degree (BSc) in Health Sciences, Biomedical Sciences, Pharmacology, or equivalent program.
- Experience: minimum of 2 years related to related experience, ideally in preclinical research.
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
WORKING ENVIRONMENT:
General working conditions in the office; the noise level is generally quiet. The employee must work under time constraints and possess the ability to deal with a variety of pressing issues on a regular basis.
Why Charles River ?
- Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage)
- Paid development training
- Employee and family assistance program
- Access to a doctor and various health professionals (telemedicine)
- Vacation & 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!
IMPORTANT: 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 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 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.
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