Scientific Support - Associate

Jobinhalt

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 seeking a Histology Data Reviewer to join our team located in Laval, QC.

The following are responsibilities related to the Data Reviewer position:

• Review data;
• Ensure that all calculations related to studies have been verified;
• Work closely with veterinarians and study directors on certain aspects of the studies;
• Provide assistance and training in data collection and reporting at all times;
• Contribute to standardization of procedures;
• Answer QA report promptly and in a clear and concise manner;
• Provide regular feedback on technician performance to their immediate supervisor, recognize and compensate good performance;
• Ensure the work environment is safe;
• Ensure study plans and amendments have been read and are understood by all technicians involved in the studies before the start of each study;
• Ensure all tasks are performed in accordance with (GLP), where applicable;
• Ensure Standard Operating Procedures (SOPs) are available, understood and constantly applied;
• Write and revise SOPs, when required;
• Participate in method development;
• Participate in new procedure implementation;
• Perform technical work, when required;
• Manage time effectively;
• Remain informed on all legislation and developments related to job through self-education and external training;
• Substitute and/or assist department colleagues;
• Perform any other reasonable tasks that may be required.
  

Job Qualifications

The following are minimum qualification required for the Data reviewer position:

• Collegial Diploma in animal health care or equivalent;
• A minimum of 3 years of relevant experience in a GLP environment;
• Practical knowledge of animal health sciences;
• Strong knowledge of related legislation, principles, practices and procedures;
• Strong knowledge and application of GLP;
• Bilingualism (French & English) is mandatory;
• Strong organizational, interpersonal and communication skills;
• Good knowledge of institutional procedures to ensure the animals well-being;
• Strong problem-solving and analytical skills;
• Ability to work under time constraint and adapt to change;
• Flexibility to work on changing work schedules;
• Ability to efficiently coordinate people, time and resources;
• Demonstrated leadership ability;
• Ability to work in a team environment;
• Working knowledge of related computer applications.
  

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 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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