Research Scientist I - Genetic Toxicology

Research Scientist I - Genetic Toxicology Req ID #:  91711 Location: 

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. Job Summary Responsible for the design, conduct and reporting of Laboratory Sciences studies efficiently, profitably and with the maximum scientific quality. The Research Scientist I/II scientifically directs the Analysts and other technical staff associated with the conduct, interpretation and reporting of studies. We are seeking a Research Scientist for our Genetic Toxicology department located in Senneville, QC.

The following are responsibilities related to theResearch Scientist: Design, write review and edit, as necessary, study plans, amendments and study schedules that define and schedule all study activities. Oversee and coordinate all aspects of study related procedures, whether performed within the department or by service departments. Ensure that projects are performed according to standard operating procedures (SOPs) and Good Laboratory Practice (GLP) regulations, and are aware of regulations published by the OECD, FDA, EPA and JMHW. Write, review and edit, as necessary, draft and/or final reports that document all study related procedures and results. The Research Scientist I/II Genetic Toxicology will be required to promptly communicate verbally or in writing with Sponsors on study related business and generate and distribute Client Interaction Reports (CIRs) in a timely manner. Ensure the accuracy and completeness of project cost estimates. Review and approve raw data, as appropriate. Ensure that a safe working environment is maintained by staff through the observance of safety procedures, the use of protective clothing and equipment, and by the distribution of relevant safety information. Notify the Senior Director, Laboratory Sciences and/or the Associate Scientific Director/Scientific Director of technical problems or deviations from budgeted costs as soon as they become apparent. Participate in the training and performance evaluation of Scientists I/II, technical staff and/or cross­ training scientific staff, where appropriate. Attend scientific meetings, symposia or workshops at the discretion of the Senior Director, Laboratory Sciences and publish or present results of the research whenever possible. Assist in the design of study packages and be able to provide advice to Sponsors on scientific issues. Perform all other related duties as assigned.

Qualifications

The following are the minimum qualifications for the role: Ph.D., D.V.M., M.Sc. or B.Sc. in an appropriate biological,chemical or related discipline. Depending on educational background, the candidate will require at least two years of experience in a relevant discipline. . An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

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 14,000 employees within 80 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 2018, revenue increased by 22% to $2.27 billion from $1.86 billion in 2017.

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 2018.

Equal Employment Opportunity 

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet

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