Charles River
Charles River utilizes an integrated approach, innovative thinking and efficiency to help you achieve your discovery program goals.
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About Charles River

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Charles River provides essential products and services to help pharmaceutical and biotechnology companies, government agencies and leading academic institutions around the globe accelerate their research and drug development efforts.

Charles River: Who We Are

Charles River Culture

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When you join Charles River, you become part of a family that has had a significant impact on the health and well-being of our families, friends and colleagues across the globe. In the past few years alone we’ve helped our clients with the critical research required to develop new, approved treatments for cancer, weight loss, cystic fibrosis, leukemia, IBS, epilepsy, Cushing’s disease and other conditions.

Working at Charles River provides you with a chance to make a difference in the world. Whether your background is in life sciences, finance, quality, IT, sales or another area, your skills will play an important role in supporting the life-saving and valuable work we perform on behalf of our clients. In return, we’ll offer you opportunities to learn, grow and build a career that you can feel passionate about.

Charles River Positions

Veterinary Pathologist II
For nearly 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 e perform. In return, we'll help you build a career that you can feel passionate about.ResponsibilitiesWe are seeking an experienced Veterinary Pathologist II for our Safety Assessment site located in Durham, NC.Responsible for independently performing gross and microscopic evaluation of tissues, recording results, preparing reports delineating pathological findings, and assisting with necropsy supervision. With minimal supervision, work with customers as needed to market company services and to assure customer satisfaction.ESSENTIAL DUTIES AND RESPONSIBILITIES:With minimal supervision, interact with clients to assure satisfaction and to market services.Perform macroscopic and microscopic tissue evaluation and interpretation of assigned studies.Enter pathology findings in data capturing system(s).Write comprehensive report narratives detailing all test article effects. As needed, work with study directors to ensure data is accurately integrated into study reports.May serve as a study director or principal investigator.May function as a peer review pathologist or may participate in a pathology working group (PWG).Provide training, technical guidance and leadership to laboratory staff and may provide training, guidance, and leadership to less experienced pathologists.May serve as a consultant in pathology-related issues.May provide scientific expertise for experimental design and other aspects of research studies as needed.Perform all other related duties as assigned.About Safety AssessmentCharles 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.    Qualifications Education:  Doctoral degree (D.V.M./V.M.D.) from an accredited veterinary school, or acceptable international equivalent in veterinary medicine.Experience: 3 or more years of pathology experience post-D.V.M.; working knowledge of clinical pathology; specialized training and/or experience in toxicologic pathology preferred.Certification/Licensure:  American College of Veterinary Pathologists (ACVP) board-certification required.Other:  Demonstrated success in technical proficiency, scientific creativity, collaboration with others and independent thought.  Works on problems of diverse scope in which analysis of data requires evaluation of identifiable factors.  Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. Computer literacy in word processing, spreadsheet and database software    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 11,000 employees within 70 facilities in 18 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 2016, revenue increased by 23.3% to $1.68 billion from $1.36 billion in 2015.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 ~70% of the drugs approved by the FDA in 2016.For more information, please visit www.criver.com.Equal Employment Opportunity Charles River Laboratories, Inc. is an Equal Opportunity Employer M/F/Disabled/VetCharles River is committed to working with and proving reasonable accomodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the employment process, please email crrecruitment_US@crl.com or call (781) 222-6244 and let us know the nature of your request and your contact information. Charles River takes affirmative action to ensure equal employment opportunity for minorities, women, disabled individuals, and covered veterans (recently separated veterans, Armed Forces service medal veterans, disabled veterans, and other protected veterans) in accordance with Executive Order 11246, Section 503 of the Rehabilitation Act of 1973 and the Vietnam Era Veterans' Readjustment Assistance Act of 1974. If you would like more information about our affirmative action program for veterans and disabled individuals, please contact Human Resources.
Veterinary Pathologist II
For nearly 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 e perform. In return, we'll help you build a career that you can feel passionate about.ResponsibilitiesWe are seeking an experienced Veterinary Pathologist II for our Safety Assessment site located in Durham, NC.Responsible for independently performing gross and microscopic evaluation of tissues, recording results, preparing reports delineating pathological findings, and assisting with necropsy supervision. With minimal supervision, work with customers as needed to market company services and to assure customer satisfaction.ESSENTIAL DUTIES AND RESPONSIBILITIES:With minimal supervision, interact with clients to assure satisfaction and to market services.Perform macroscopic and microscopic tissue evaluation and interpretation of assigned studies.Enter pathology findings in data capturing system(s).Write comprehensive report narratives detailing all test article effects. As needed, work with study directors to ensure data is accurately integrated into study reports.May serve as a study director or principal investigator.May function as a peer review pathologist or may participate in a pathology working group (PWG).Provide training, technical guidance and leadership to laboratory staff and may provide training, guidance, and leadership to less experienced pathologists.May serve as a consultant in pathology-related issues.May provide scientific expertise for experimental design and other aspects of research studies as needed.Perform all other related duties as assigned.About Safety AssessmentCharles 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.    Qualifications Education:  Doctoral degree (D.V.M./V.M.D.) from an accredited veterinary school, or acceptable international equivalent in veterinary medicine.Experience: 3 or more years of pathology experience post-D.V.M.; working knowledge of clinical pathology; specialized training and/or experience in toxicologic pathology preferred.Certification/Licensure:  American College of Veterinary Pathologists (ACVP) board-certification required.Other:  Demonstrated success in technical proficiency, scientific creativity, collaboration with others and independent thought.  Works on problems of diverse scope in which analysis of data requires evaluation of identifiable factors.  Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. Computer literacy in word processing, spreadsheet and database software    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 11,000 employees within 70 facilities in 18 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 2016, revenue increased by 23.3% to $1.68 billion from $1.36 billion in 2015.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 ~70% of the drugs approved by the FDA in 2016.For more information, please visit www.criver.com.Equal Employment Opportunity Charles River Laboratories, Inc. is an Equal Opportunity Employer M/F/Disabled/VetCharles River is committed to working with and proving reasonable accomodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the employment process, please email crrecruitment_US@crl.com or call (781) 222-6244 and let us know the nature of your request and your contact information. Charles River takes affirmative action to ensure equal employment opportunity for minorities, women, disabled individuals, and covered veterans (recently separated veterans, Armed Forces service medal veterans, disabled veterans, and other protected veterans) in accordance with Executive Order 11246, Section 503 of the Rehabilitation Act of 1973 and the Vietnam Era Veterans' Readjustment Assistance Act of 1974. If you would like more information about our affirmative action program for veterans and disabled individuals, please contact Human Resources.
Document & Laboratory Control Specialist
For nearly 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.We are seeking an experiencedDocument & Laboratory Control Specialist for ourInsourcing Solutionssite located in New Haven, CT.Your primary role, facilitates overall laboratory compliance within cGLP and research labs. Provides oversight to other third party lab and technical service providers to ensure Service Level Agreements (SLA's) meet regulatory requirements, as well as the needs of the client. Monitors and ensures the delivery of preventative and corrective maintenance, warranty coverage and calibration for all laboratory equipment and instrumentation. Coordinates IQ/OQ/PQ of applicable instrumentation as well as represents the research business owner of validation project teams. The role will support GLP document lifecycle management and broadly support multiple research functions with Environmental Health and Safety (EHS) and Radiation Compliance (RAD).The following are minimum requirements related to theDocument & Laboratory Control Specialist position.Education: Bachelor's degree (B.S.) in life sciences field.Experience: 7 or more years of direct technical experience within a scientific research laboratory environment. Proven experience demonstrating knowledge, skills and abilities required to perform the role. General understanding of ISO/IEC 17025 accredited calibrations, NVLAP, NIST, GLPs, GMPs, GDPs, and concepts of IQ, OQ and PQ qualification services is required.About Insourcing Solutions Charles River Insourcing Solutions can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment. Insourcing Solutions provides you with the ability to maintain control of your facility and expertise while leveraging available space.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 11,000 employees within 70 facilities in 18 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 2016, revenue increased by 23.3% to $1.68 billion from $1.36 billion in 2015.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 ~70% of the drugs approved by the FDA in 2016.For more information, please visit www.criver.com.Equal Employment Opportunity Charles River Laboratories, Inc. is an Equal Opportunity Employer M/F/Disabled/VetCharles River is committed to working with and proving reasonable accomodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the employment process, please email crrecruitment_US@crl.com or call (781) 222-6244 and let us know the nature of your request and your contact information. Charles River takes affirmative action to ensure equal employment opportunity for minorities, women, disabled individuals, and covered veterans (recently separated veterans, Armed Forces service medal veterans, disabled veterans, and other protected veterans) in accordance with Executive Order 11246, Section 503 of the Rehabilitation Act of 1973 and the Vietnam Era Veterans' Readjustment Assistance Act of 1974. If you would like more information about our affirmative action program for veterans and disabled individuals, please contact Human Resources.
Document & Laboratory Control Specialist
For nearly 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.We are seeking an experiencedDocument & Laboratory Control Specialist for ourInsourcing Solutionssite located in New Haven, CT.Your primary role, facilitates overall laboratory compliance within cGLP and research labs. Provides oversight to other third party lab and technical service providers to ensure Service Level Agreements (SLA's) meet regulatory requirements, as well as the needs of the client. Monitors and ensures the delivery of preventative and corrective maintenance, warranty coverage and calibration for all laboratory equipment and instrumentation. Coordinates IQ/OQ/PQ of applicable instrumentation as well as represents the research business owner of validation project teams. The role will support GLP document lifecycle management and broadly support multiple research functions with Environmental Health and Safety (EHS) and Radiation Compliance (RAD).The following are minimum requirements related to theDocument & Laboratory Control Specialist position.Education: Bachelor's degree (B.S.) in life sciences field.Experience: 7 or more years of direct technical experience within a scientific research laboratory environment. Proven experience demonstrating knowledge, skills and abilities required to perform the role. General understanding of ISO/IEC 17025 accredited calibrations, NVLAP, NIST, GLPs, GMPs, GDPs, and concepts of IQ, OQ and PQ qualification services is required.About Insourcing Solutions Charles River Insourcing Solutions can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment. Insourcing Solutions provides you with the ability to maintain control of your facility and expertise while leveraging available space.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 11,000 employees within 70 facilities in 18 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 2016, revenue increased by 23.3% to $1.68 billion from $1.36 billion in 2015.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 ~70% of the drugs approved by the FDA in 2016.For more information, please visit www.criver.com.Equal Employment Opportunity Charles River Laboratories, Inc. is an Equal Opportunity Employer M/F/Disabled/VetCharles River is committed to working with and proving reasonable accomodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the employment process, please email crrecruitment_US@crl.com or call (781) 222-6244 and let us know the nature of your request and your contact information. Charles River takes affirmative action to ensure equal employment opportunity for minorities, women, disabled individuals, and covered veterans (recently separated veterans, Armed Forces service medal veterans, disabled veterans, and other protected veterans) in accordance with Executive Order 11246, Section 503 of the Rehabilitation Act of 1973 and the Vietnam Era Veterans' Readjustment Assistance Act of 1974. If you would like more information about our affirmative action program for veterans and disabled individuals, please contact Human Resources.
Shipping and Receiving Supervisor
For nearly 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 e perform. In return, we'll help you build a career that you can feel passionate about.ResponsibilitiesWe are seeking an experienced Shipping and Receiving Supervisor for our Discovery site located in Worcester.This position is a hands-on management position which will be responsible for the receiving of goods and shipment of outgoing materials. This position is responsible for the reconciliation of goods and service receipts within SAP and management of the discrepancy report.  This position will have direct and matrixed reports.  Coordinate courier deliveries and shipments, and manage the courier relationship.  Oversee packaging of materials according to IATA or DOT dangerous goods regulations. Oversee special projects including international shipments, CITES, US Fish and Wildlife, and CDC projects. The following are minimum requirements related to the Shipping and Receiving Supervisor position. QUALIFICATIONS:Education:   High school diploma or General Education Degree (G.E.D.) required. Associate’s degree (A.A./A.S.) or equivalent in a related field preferred.Experience:   3-5 years of shipping experience is required; experience handling hazardous materials preferred. Leadership 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:    Must have a valid driver’s license and verified clean driver’s abstract.  IATA and DOT certification preferred and ability to pass certification within 90 days required.Other:  Must be knowledgeable in IATA and DOT shipping regulations. Must possess excellent organizational skills and the ability to manage multiple priorities; computer literacy with database and word processing skills; the ability to interact appropriately with all levels of staff and attention to detail. Must possess effective supervisory and communication skills and ability to gain cooperation from others.  About DiscoveryDiscovery from Charles River is industry-proven in the successful development of novel therapies, with over 320 patents and 74 preclinical drug candidates delivered to our sponsors in the past 17 years. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND. Our client-focused, collaborative approach creates true partnerships that anticipate challenges, overcome obstacles, and move us forward together on the journey of getting new drugs to market.About Charles RiverCharles 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 11,000 employees within 70 facilities in 18 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 2016, revenue increased by 23.3% to $1.68 billion from $1.36 billion in 2015.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 ~70% of the drugs approved by the FDA in 2016.For more information, please visit www.criver.com.Equal Employment OpportunityCharles River Laboratories, Inc. is an Equal Opportunity Employer M/F/Disabled/VetCharles River is committed to working with and proving reasonable accomodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the employment process, please email crrecruitment_US@crl.com or call (781) 222-6244 and let us know the nature of your request and your contact information. Charles River takes affirmative action to ensure equal employment opportunity for minorities, women, disabled individuals, and covered veterans (recently separated veterans, Armed Forces service medal veterans, disabled veterans, and other protected veterans) in accordance with Executive Order 11246, Section 503 of the Rehabilitation Act of 1973 and the Vietnam Era Veterans' Readjustment Assistance Act of 1974. If you would like more information about our affirmative action program for veterans and disabled individuals, please contact Human Resources.
Shipping and Receiving Supervisor
For nearly 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 e perform. In return, we'll help you build a career that you can feel passionate about.ResponsibilitiesWe are seeking an experienced Shipping and Receiving Supervisor for our Discovery site located in Worcester.This position is a hands-on management position which will be responsible for the receiving of goods and shipment of outgoing materials. This position is responsible for the reconciliation of goods and service receipts within SAP and management of the discrepancy report.  This position will have direct and matrixed reports.  Coordinate courier deliveries and shipments, and manage the courier relationship.  Oversee packaging of materials according to IATA or DOT dangerous goods regulations. Oversee special projects including international shipments, CITES, US Fish and Wildlife, and CDC projects. The following are minimum requirements related to the Shipping and Receiving Supervisor position. QUALIFICATIONS:Education:   High school diploma or General Education Degree (G.E.D.) required. Associate’s degree (A.A./A.S.) or equivalent in a related field preferred.Experience:   3-5 years of shipping experience is required; experience handling hazardous materials preferred. Leadership 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:    Must have a valid driver’s license and verified clean driver’s abstract.  IATA and DOT certification preferred and ability to pass certification within 90 days required.Other:  Must be knowledgeable in IATA and DOT shipping regulations. Must possess excellent organizational skills and the ability to manage multiple priorities; computer literacy with database and word processing skills; the ability to interact appropriately with all levels of staff and attention to detail. Must possess effective supervisory and communication skills and ability to gain cooperation from others.  About DiscoveryDiscovery from Charles River is industry-proven in the successful development of novel therapies, with over 320 patents and 74 preclinical drug candidates delivered to our sponsors in the past 17 years. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND. Our client-focused, collaborative approach creates true partnerships that anticipate challenges, overcome obstacles, and move us forward together on the journey of getting new drugs to market.About Charles RiverCharles 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 11,000 employees within 70 facilities in 18 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 2016, revenue increased by 23.3% to $1.68 billion from $1.36 billion in 2015.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 ~70% of the drugs approved by the FDA in 2016.For more information, please visit www.criver.com.Equal Employment OpportunityCharles River Laboratories, Inc. is an Equal Opportunity Employer M/F/Disabled/VetCharles River is committed to working with and proving reasonable accomodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the employment process, please email crrecruitment_US@crl.com or call (781) 222-6244 and let us know the nature of your request and your contact information. Charles River takes affirmative action to ensure equal employment opportunity for minorities, women, disabled individuals, and covered veterans (recently separated veterans, Armed Forces service medal veterans, disabled veterans, and other protected veterans) in accordance with Executive Order 11246, Section 503 of the Rehabilitation Act of 1973 and the Vietnam Era Veterans' Readjustment Assistance Act of 1974. If you would like more information about our affirmative action program for veterans and disabled individuals, please contact Human Resources.
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