Charles River Labs
Data Reviewer - Immunology
This job is now closed
Job Description
- Req#: 216332
- Guarantee accurate review and corrections in accordance with Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP) and study plans.
- Ensure that all pertinent data is reviewed.
- Ensure that the review and corrections are finalized according to established due dates.
- Proactive in obtaining answers to findings. Responsible for documenting any remaining issues at data review clearance
- DEC in sciences or AEC
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
- Be able to work in team. Have a positive attitude. Adapt to changes.
- Regularly operates a computer and other office productivity machinery.
- Must be able to remain in a stationary position at least 80% of the time.
- Competitive benefits upon hire. We pay up to 85% of premiums (medical & dental coverage)
- Paid development training
- Employee and family assistance program
- 24/7 access to a doctor and various health care professionals (telemedicine)
- 3 weeks’ Vacation & 5 Personal day policy
- Numerous organized social activities
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
As a Data reviewer for our Immunology team located at the Senneville site, you will do verification of raw data according to Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP), and study plans.
In this role, responsibilities may include:Key Elements
We are looking for the following minimum qualifications for this role:
Role Specific Information
Location: Senneville or Ville St-Laurent , (Shuttle service from Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site), Free parking
Salary: Starting at $19.50/hr. Possibility of starting at a higher level with specific research experience
Schedule: weekday schedule, Monday to Friday
Permanent position upon hiring, full time at 37.5hrs per week
Why Charles River?
If you want to contribute to the well-being of our communities, not only across the country, but around the world, join the team, IT'S YOUR MOMENT!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.
For more information, please visit www.criver.com.
About the company
Charles River Laboratories, Inc., is an American corporation specializing in a variety of preclinical and clinical laboratory services for the pharmaceutical, medical device and biotechnology industries.