Scheduling - Associate (Remote)

Scheduling - Associate (Remote) Req ID #:  197893 Location: 

Laval, Quebec, CA, H7V 4B3 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 We are currently seeking to hire a scheduling associate for our Reporting Services team located in Laval.  

How will you create an impact?

The Reporting Services department serves to offer quality service to our clients by issuing high-quality study reports.

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:

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

Transportation: Shuttle service from the Montmorency Metro Station to the Laval location. Free parking.

Work Schedule & Salary: Starting salary rate of $22/HR. Permanent, full-time position from Monday to Friday. Opportunity to work from home. 

  Job Qualifications As a Scheduling associate , you will Create studies in Report Progress Monitoring (RPM) and in the Master Schedule, m aintain the Report Progress Monitoring (RPM) database and the Master Schedule up to date  , ensure all milestones (in life and reporting) are respected, interact with Study Directors, Scientists and/or all departments to clarify information and resolve any issues related to scheduling and reporting , produce various report (weekly, monthly, quarterly and annually)

Who are we looking for?

We are seeking a motivated individual with a DEC (Office Technologies or equivalent) who works with accuracy, precision, and who strives for quality work. A self-starter with a collaborative and positive attitude. Must be comfortable working under English conditions, bilingualism is an asset.  

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 and BE THE DIFFERENCE! 

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 20,000 employees within 110 facilities in over 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.

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 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

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 crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.

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