Research Associate - Laval, Canada - Charles River Laboratories

Sophia Lee

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Sophia Lee

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Description

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:

We are looking for a
Research Associate to join our Toxicology team located in
Laval - Temporary position.


How will you make an impact?


As a Research Associate, you will be the central point of communication from the beginning to the end of the study.

Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.


Why work at Charles River?
We offer an excellent onboarding program for our new employees as well as many opportunities for internal development.


As of day 1:

  • Vacation policy and personal days off

Transport:


  • Public transport service to the Laval site
  • Free parking

Salary:


  • Hourly rate based on experience
  • After 37,5h : Overtime paid at time and a half
  • Temporary fulltime position
  • Schedule between Monday to Friday daytime, 37.5 hours per week

What will you be working on?


You will be required to
review the study plans and
discuss the specific needs for the studies with the scientist.

You will also be called to
schedule the training and the equipment necessary to carry out the studies.

Finally, you will have to
collaborate, coordinate and communicate effectively with the technical teams, the Study Directors, the Veterinarians and other departments to ensure the smooth running of the studies.


Who are we looking for?


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

If you want to contribute to the well-being of our communities, not only across the country, but around the world, join the team and BE THE DIFFERENCE


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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