Site Clerk, Scientific Coordination, Lab Sci Job at Charles River Laboratories
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
We are seeking a Summer Site Clerk for our Safety Assessment site located in Reno, NV.
The Site Clerk will perform basic tasks as outlined by the supervisor to provide support/assistance to assigned department(s). Some of the responsibilities may include but not limited to: General housekeeping and maintenance of department areas; wash, sterilize, and prepare glassware for laboratory use; prepare basic documentation, labeling and or other records keeping and filing; and perform all other related duties as assigned.
Job Qualifications
The following are minimum requirements related to the Site Clerk position:
- Availability to work full-time (40 hours), day shift Monday through Friday; 6 month Temporary role
- High school diploma or General Education Degree (G.E.D.)
- 0-6 months related experience
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
- Ability to organize, prioritize work and meet deadlines. Must be detail oriented.
About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.
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