For 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.

JOB SUMMARY

We are seeking a RESEARCH ASSISTANT I(2nd Shift 1:00 pm to 9:00 pm) for our Safety Assessment Group site located in ASHLAND, OHIO.

Generate 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.

• Perform 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.
• Under supervision may act as lead/primary technician on basic studies.
• Input, print and edit computer entries (e.g., laboratory data).
• Prepare materials and data for shipment and archiving.
• Receive samples and complete tracking documentation.
• Review documentation of functions performed as part of quality control requirements.
• Perform study preparation activities including collection tube labeling and room setup.
• Maintain clean work areas.
• Perform all other related duties as assigned.

The following are miminum requirements related to the RESEARCH ASSISTANT I position.

• Education: Bachelor’s degree (B.A. / B.S) or equivalent in laboratory science or related discipline required.
• Experience: Zero to two years related experience in biology, chemistry/pharmacy, or similar lab environment GLP experience preferred.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: None
• Other: 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 experience preferred.

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 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

ABOUT CHARLES RIVER

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.

With over 14,000 employees within 80 facilities in 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. And in 2018, revenue increased by 22% to $2.27 billion from $1.86 billion in 2017.

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 ~85% of the drugs approved by the FDA in 2018.

EQUAL EMPLOYMENT OPPORTUNITY

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet

NEAREST MAJOR MARKET: Cleveland

NEAREST SECONDARY MARKET: Mansfield

JOB SEGMENT: Toxicology, Biotech, Research Assistant, Pharmaceutical, Science, Research

Charles River Laboratories is a visionary leader in the development and delivery of advanced drug therapies. We provide essential products and services to pharmaceutical and biotechnology companies, government agencies and leading academic institutions around the globe, to help accelerate their research and drug development efforts. At Charles River, we view every day as an opportunity to improve global health and people's lives. Our dedicated employees are focused on providing clients with exactly what they need to improve and expedite the discovery, early-stage development and safe manufacture of new therapies for the patients who need them.