Research Scientist I, Toxicology

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. Serve as a scientist in the conduct of assigned nonclinical research studies of basic to moderate complexity.

Requirements

• Serve as a study director in the direction and execution of assigned studies in compliance with GLP regulations as they apply to the conduct of nonclinical research.
• Participate in proposal management and bid development process.
• Generate high-quality protocols, amendments, and reports appropriate for assigned studies.
• Review, interpret, integrate, and present data on assigned studies, using the assistance of senior scientific staff as appropriate.
• Function as contact for the planning and execution of sponsor interaction related to assigned studies, including proposal management and study scheduling, conduct and reporting.
• Provide technical and scientific guidance to the research staff.
• Attend scientific meetings, conferences, and training courses to enhance job and professional skills.

Benefits

• bonus/incentives based on performance
• 401K
• paid time off
• stock purchase program
• Health and wellness coverage
• employee and family wellbeing support programs
• work life balance flexibility