Report Finalization Support Scientist - Toxicology Reporting

Req ID #:  102752

Senneville, Quebec, CA, H9X 3R3

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 looking for a Report Finalization Support Scientist to assist the Study Directors with the administrative tasks involved with the finalization of reports for our site in Senneville.


The responsibilities are the following: 
•    Provides administrative support to Study Directors and/or Report Finalization Scientist for the finalization process of reports 
•    Autonomously manages the receipt, distribution, and pursue of report comments received with judgment and accuracy
•    Coordinate and collaborate with involved departments to ensure report comments are executed as described above  
•    Prioritize his/her workload to manage the concomitant organization of report comments 
•    Required to regularly maintain the tracking tool of the received report comments 
•    May assist with management of Quality Assurance (QA) audits

Job Qualifications


The  minimum requirements are:
•    Minimum of a Bachelor’s degree (BA/BS) or equivalent. Experience: 1 to 3 years of related industry experience considered an asset
•    An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
•    Functions as an independent administrative/logistics support to the Study Director and/or Report Finalization Scientist in accordance with Standard Operating Procedures and Good Laboratory Practice regulations and is aware of appropriate regulations, guidelines and guidance of the applicable Good Laboratory Practices (GLPs) 
•    Understands the reporting process
•    Knowledge of Quality Assurance (QA)/Quality Control (QC) process
•    Prompt and effective verbal or written communication with internal clients on study-related items in a manner that generates confidence and builds trust
•    Proven experience of working within given timescales with excellent attention to detail and demonstrated organizational skills
•    Demonstrates ability to prioritize daily tasks
•    Demonstrates ability to use critical thinking to anticipate and resolve study-related issues
•    Basic familiarity with Microsoft Office Suite



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 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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