Research Assistant I - Analytical Chemistry

About the role

The Research Assistant, Analytical Chemistry will be responsible for generating and recording data with minimal supervision in the performance of studies. He/she/they will be responsible for handling and processing samples and performing accurate data collection and reporting as well as performing laboratory tasks by various basic methods.

Responsibilities

• 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.
• 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.
• Maintain clean work areas.
• Perform all other related duties as assigned.

Qualifications

• 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 in a contract lab, or similar lab environment GLP experience preferred.
• 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.

Pay

The pay range for this position is between $23.00 and $24.00 an hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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.

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.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.