Scientist - Study Management

Req ID #: 225023

Laval, QC, CA

Full time

For 75 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**

As a **Scientist **for our **Toxicology** team located in **Laval**, you will be responsible for overseeing study conduct of preclinical efficacy and/or toxicology studies. Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.

In this role, primary **responsibilities** include:

- Function as an independent Study Director in accordance with the applicable Good Laboratory Practices (GLPs)
- Designs, writes, reviews and edits, as necessary, Study Plans, amendments and study schedules that define and schedule all study activities
- Oversees and coordinates all aspects of study procedures, whether performed within the department or by service departments
- Ensures that projects are performed according to Standard Operating Procedures and Good Laboratory Practice regulations and is aware of appropriate regulations, guidelines and guidances
- Writes, reviews, and edits, as necessary, draft or final reports that document all study related procedures and results
- Prompt verbal or written communication with Sponsors on study related business
- Oversees and coordinates study conduct (protocol development, technical guidance, and reporting)

**Key Elements**

We are looking for the following **minimum qualifications** for this role:

- Master’s or Doctorate in Pharmacology, Toxicology, or any other related discipline
- Technical certificate in MRI (Magnetic Resonance Imaging) is an asset
- Communication, writing and reading comprehension in English is mandatory. Bilingualism in French and English is preferred
- Good interpersonal and communication skills
- Strong problem-solving skills
- MRI (Magnetic Resonance Imaging) experience is an asset

**Role Specific Information**:

- Location: Laval / Free parking / Near the subway Montmorency
- Annual bonus based on performance
- Schedule: Monday to Friday, 8:00 am to 4:15 pm
- Hybrid position - half on-site & half remote
- Permanent position as of the hiring, full-time 37.5hrs per week

**Why Charles River ?**
- Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage)
- Paid development training
- Employee and family assistance program
- Excellent welcome program for new employees as well as in-house advancement and career development opportunities
- Access to a doctor and various health professionals (telemedicine)
- Vacation & Personal day policy
- Many social activities

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. **This is Your Moment.**

**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 300 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.

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 worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

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