Study Coordinator

Job type: Full-Time
Accepting BioReady™: Yes
Category: Research and Development
Education: Diploma/DEC
Experience: 0-3 Years
Location: Montreal (Senneville), QC
Posted: September 22, 2022
Closes: October 22, 2022

For 70 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.

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

We are currently seeking to hire a Study Coordinator for our Lab Science department. This is a full time work from home opportunity.

Why Charles River? 

We offer an excellent integration program for our new employees as well as opportunities for internal growth and career development.

Our other perks include:

  • Competitive benefits & we pay 90% of premiums (health and dental coverage) as of day 1.
  • Access to a savings and retirement program with employer contribution.
  • 3 weeks Vacation and 5 Personal Day Policy.
  • Free telemedicine app for you and your family.

Work Schedule:

  • Permanent, full-time work from home position, from Monday to Friday.

What will you work on?

  • Schedule and monitor study milestones using appropriate software applications (RPM, Front End).
  • Process study related documents; including processing signature/approval of study plan/amendments, distribution of draft/final study plan/amendments, and corresponding with sponsors to ensure regulatory documents are signed and returned.
  • Review study related documents (study plans/amendments) upon issuance to assure full understanding of assigned projects to assess impact on timelines and reporting requirements.
  • Responsible to ensure that all original study plan/amendment and related documents are transferred to the appropriate individual for filing.
  • Other individual tasks as delegated by Supervisor to ensure departmental work flow

Who are we looking for?

  • Education: DEC.
  • An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe et SOYEZ LA DIFFÉRENCE!

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.

About Charles River

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 17,000 employees within 90 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of ~85% of the drugs approved by the FDA in 2019.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer – M/F/Disabled/Vet.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to [email protected] This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

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