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.

KEY REQUIRED SKILLS AND EDUCATION:

• Minimum of Master level education in biology, veterinary medicine, agricultural or similar
• (in special cases B.Sc. degree can be also accepted)
• 1-3 years of professional experience (preferred, but not mandatory)
• Good verbal and written communication skills and superior customer service skills
• High degree of self-motivation with effective organizational and time management skills
• High level spoken and written English required
• Computer skills including Word, EXCEL, Powerpoint

• Respective specialities: mammalian toxicology or in vitro toxicologyy
• Key role in management of preclinical studies or regulatory toxicity studies
• Study set- up, study plan, study conduct and supervision
• Oversight of data collection, interpretation, analysis, documentation, and reporting of results; and the derivation, of study conclusions
• Responsible for the conduct of the good technical aspects of the study phase and/or the data evaluation, reporting and sharing any study related event with the responsible Study Director during the delegated phase
• Coordination of the study team
• Review of the study documentation, data evaluation, study report
• Close collaboration with internal departments and external partners
• Work in compliance with applicable GLP, ISO and SOPs.