Scientist - Study Management Professional
3 weeks ago
For 75 years, Charles River has been a leading CRO in assisting the discovery, development, and safe manufacture of new drug therapies.
About Charles RiverWe are an early-stage contract research organization (CRO) with a diverse portfolio of discovery and safety assessment services.
Our mission is to improve the quality of people's lives by helping our clients expedite their preclinical drug development.
We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.
Key Responsibilities- 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
- Master's or Doctorate in Pharmacology, Toxicology, or any other related discipline
- Communication, writing and reading comprehension in English is mandatory. Bilingualism in French and English is preferred
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
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