Research Technician – Rapid Response Team

Job type: Full-Time
Accepting BioReady™: Yes
Category: Preclinical Research
Salary:
Location: Montreal, QC
Posted: June 11, 2019
Ends: July 11, 2019

Job description:

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.

We are looking for Technicians at all skill levels who have an adventurous spirit and specialize in Research to join our Rapid Response teams.  In this role, you will have the opportunity for paid travel to various North American and global Charles River sites, performing basic and advanced laboratory procedures. You will have the opportunity to expand your skills and cross train in various techniques while meeting new Charles River colleagues.  This is an exciting opportunity for those willing to travel with minimal notice.  Home base for these positions may be located at any of our Charles River sites. We are also open to remote employees.

Travel required is 75% or more.

 

Essential Duties and Responsibilities:

Research Technicians

Responsible for performing technical tasks in the conduct of in vivo research studies or support services in accordance with good animal welfare practices. Will prepare, collect and record research data and specimens in compliance with applicable regulations and SOPs.  Will collect and record data with minimal supervision in the performance of studies.   Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods.  ALAT certification preferred.

 

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 13,000 employees within 80 facilities in 23 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 80% of the drugs approved by the FDA in 2017.

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

 

Interested candidates are asked to apply by clicking this link.