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

Serve as a scientist in the conduct of assigned nonclinical research studies of basic to moderate complexity, to include study management, interpretation and reporting of study data, and assuring the regulatory compliance of these projects.

JOB QUALIFICATIONS

Education: Ph.D. or equivalent in toxicology or related scientific related discipline.

• Experience: 0 – 1 year.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: N/A.
• Other: Understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and the Good Laboratory Practices (GLPs), as appropriate. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc. and with standard laboratory calculations.

• 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. Assist in the review of Letters of Commitment (LOC) in cooperation with client services.
• Participate in and coordinate all phases of the study planning process with appropriate departments.
• 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.
• Perform all other related duties as assigned.