For nearly 70 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.
We are seeking an experienced Report Coordinator for our Safety Assessment] site located in Reno, NV.
The Report Coordinator will be responsible for publishing scientific data tables and establishing the framework of reports. The Report Coordinator will be developing the Introduction and Methods sections of Draft Reports for Charles River Laboratories, Safety Assessment studies.
The following are minimum requirements related to the Report Coordinator position.
- Associate’s degree (A.A./A.S.) in journalism, computer science, business administration or related discipline.
- 3-5 years related experience in scientific data presentation, writing, editing, proofreading and publishing.
- Proficient with spreadsheet, database, and publishing software (e.g. MS Excel®, Word®, and Adobe® Acrobat® PDF software). Proficient at file conversion and compilation. Strong written, verbal, and analytical skills. Familiar with medical terminology. Familiar with preclinical study protocols/reports and FDA Electronic Reporting compliance preferred. Familiarity with Provantis™ system and/or Business Objects preferred.
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Equal Employment Opportunity
Charles River Laboratories, Inc. is an Equal Opportunity Employer M/F/Disabled/Vet