Research Analyst I, Bioanalytical Chemistry (Ashland, OH, US, 44805)

pspan style="font-size:10.0px"span style="font-family:Arial, Helvetica, sans-serif"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./span/span/p divdiv style="padding:10.0px 0.0px;border:1.0px solid transparent"div style="font-size:16.0px;word-wrap:break-word"H2 style="font-size:1.0em;margin:0.0px"bJob Summary/b/H2 /divdivpWe are seeking a bResearch Analyst I (Bioanalytical Chemistry)/b for our Safety Assessment Group site located in bAshland, Ohio./b/p p /p pGenerate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples and performing accurate data collection and reporting. Perform laboratory tasks by various basic methods./p p /p ul liPerform basic laboratory procedures and collect and record/document research data in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), study protocols and company policies/practices./li liUnder supervision may act as lead/primary technician on basic studies./li liBasic Understand/Knowledge LCMS/li liInput, print and edit computer entries (e.g., laboratory data)./li liPrepare materials and data for shipment and archiving./li liReceive samples and complete tracking documentation./li liReview documentation of functions performed as part of quality control requirements./li liPerform study preparation activities including collection tube labeling and room setup./li liMaintain clean work areas./li liPerform all other related duties as assigned./li /ul p /p pThe following are miminum requirements related to the bResearch Assistant I /bposition. /p ul liEducation:  Bachelor’s degree (B.A. / B.S) or equivalent in laboratory science or related discipline required./li liExperience:  Zero to two years related experience in biology, chemistry/pharmacy, or similar lab environment GLP experience preferred./li liAn equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above./li liCertification/Licensure:  None/li liOther:  Proficient in basic technical skills and the operation of data collection equipment. Knowledge of GLPs and other federal regulations and guidelines. Basic understanding of study design and protocols; able to read basic study protocols and extract pertinent information. Must be able to perform effectively as a team member, accurately record data, follow verbal and written instructions, communicate effectively, and interact in a professional manner with management, coworkers, and sponsors. Able to quickly learn and utilize computer programs as needed; previous computer experiences preferred./li /ul pbThe pay range for this position is $21.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location/b/p p /p /div/div/divpspan style="font-size:10.0px"span style="font-family:Arial, Helvetica, sans-serif"bAbout Safety Assessment/bbr 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./span/span/p p /p pbr span style="font-size:10.0px"span style="font-family:Arial, Helvetica, sans-serif"bAbout Charles River/bbr Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market./span/span/p p /p pspan style="font-size:10.0px"span style="font-family:Arial, Helvetica, sans-serif"With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world./span/span/p p /p pspan style="font-size:10.0px"span style="font-family:Arial, Helvetica, sans-serif"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. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021./span/span/p p /p pspan style="font-size:10.0px"span style="font-family:Arial, Helvetica, sans-serif"bEqual Employment Opportunity/b/span/span/p pspan style="font-size:10.0px"span style="font-family:Arial, Helvetica, sans-serif"Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status./span/span/p p /p pspan style="font-size:10.0px"span style="font-family:Arial, Helvetica, sans-serif"If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications./span/span/p p /p pspan style="font-size:10.0px"span style="font-family:Arial, Helvetica, sans-serif"For more information, please visit www.criver.com./span/span/p