Research Analyst 1 -Bio/Immunology 1
Charles River Laboratories International Inc (CRL)
Reno, NV, US, 89511
Research Analyst 1 -Bio/Immunology 1 Req ID #: 194616 Location:
Reno, NV, US, 89511 At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.
Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.
As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe.
IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly.
We are seeking a Research Assistant 1 for our Safety Assessment site located in Reno, NV.
This position will be responsible for handling and processing samples, and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies. Job Qualifications
The following are minimum requirements related to the Research Assistant 1 position.
Associate's degree (A.A. / A.S) or equivalent in biological science or related discipline required. Bachelor’s degree (B.A. / B.S.) preferred. 6 Months minimum 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. 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.
IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.
About Corporate Functions
The Corporate Functions provide operational support across Charles River in areas such as Human Resources, Finance, IT, Legal, Sales, Quality Assurance, Marketing, and Corporate Development. They partner with their colleagues across the company to develop and drive strategies and to set global standards. The functions are essential to providing a bridge between strategic vision and operational readiness, to ensure ongoing functional innovation and capability improvement.
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 17,000 employees within 90 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 2019, revenue increased to $2.62 billion.
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 2019.
Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.
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 [email protected] This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit www.criver.com.
Nearest Major Market: Reno
Nearest Secondary Market: Tahoe
Job Segment: Pharmaceutical, Research Assistant, Laboratory, Quality Assurance, Research, Science, Technology
Similar CRA jobs
Research Assistant 1 - Immunoassay
Clinical Research Administrative Assistant, English and French mandatory
Resource Analyst - IRD
RWI Data Analyst
Lab Clinical Data Analyst, based in Hounslow, London
Finance Analyst II
(Senior) Clinical Research Associate - Netherlands
Research Scientist 1- Oncology
Research Associate (Phlebotomist) (Chinese or Japanese Fluent)
Contract, Sr. Clinical Research Associate, Surgical/Gastrointestinal (Central US Sites) - IQVIA Biotech
Feasibility Informatics Analyst
Business Analyst / Solution Architect
Validation Analyst, Labs (Monday-Friday 9a-530p)
Research Technician I, Technical Operations
Sr Application Support Analyst
Clinical Research Associate II - Southeast
Sr. Research Scientist, Bioanalytical Chemistry
Senior Clinical Research Associate, Oncology/Medical Device/Dermatology (Poland - home based) - IQVIA Biotech
Senior Research Scientist- CE-MS or CE experience
Sr. Clinical Research Associate, Cardiology or Renal studies; West US, IQVIA Biotech