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Charles River

Research Scientist I

Post Date:Apr 16, 2018Type:Full-Time
Start Date:4/16/2018Salary:
Location:US-OH-Ashland Job Reference:31923
Skills:
  • Education: Ph.D. in analytical chemistry or MS with 5-7 years of experience in regulated bioanalysis or BS with 8-10 years of experience.  Candidates with more experience will be considered for higher level positions.
  • 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.

     



Job Description:
About the Company:

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe.

Our collective efforts as One Charles River are the key to our success, and we know that every person is important. Every day, each of us plays a critical role in making a difference in the quality of people's lives.
From our animal technicians and security guards to our business managers and executive team, we’re working together to support better, safer and more effective research. 

BASIC SUMMARY:  

Serve as a Principal Investigator on bioanalytical studies. This includes study management, interpretation and reporting of study data, and assuring the regulatory compliance of these projects.

 

ESSENTIAL DUTIES AND RESPONSIBILITIES:  

  • Serve as a study director/principal investigator in the direction and execution of assigned studies in compliance with GLP regulations as they apply to the conduct of nonclinical research.
  • Interfaces with customers to understand the scientific and regulatory requirements for preclinical and clinical bioanalysis studies.
  • 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.





Contact Information
Charles River



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