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.
Requirements
- Function independently as a Project Scientist, Principal Investigator, Contributing Scientist in the direction and execution of assigned studies in compliance with regulations as they apply to the conduct of preclinical and clinical research.
- Participate in and coordinate all phases of the study planning process with appropriate departments.
- Develop assays, generate high-quality laboratory method, protocols, amendments, reports, and facilitate appropriate changes to study design for assigned projects and programs.
- Review, interpret, integrate, and present data on assigned studies.
- Writes and edits draft or final reports that document all study related procedures and results.
- Analyze scientific problems, troubleshoot analytical methods and technical issues.
- Function independently as the point of contact for the planning and execution of sponsor interaction related to assigned studies, including proposal management and study scheduling, conduct and reporting.
- Provide prompt verbal or written communication with Sponsors on study related business.
- Mentor technical staff in areas such as protocol interpretation, method development and refinement, study-related problem resolution, and execution of validation studies.
- Provide technical and scientific guidance to the research staff.
- Contribute to testing of new biomarker technologies or introduce improvements in existing technologies.
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