Scientist - Study Management

at  Charles River Laboratories

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

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

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 asse