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

Project Manager III
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 experience Project Manager III for ourInsourcingSolutionssite located in Atlanta, GA. Indiviaul plans, organizes and directs the activities of the animal husbandry program atcontract site. Manages a staff of area supervisors, veterinary technicians, animal care technicians, cage wash technicians, and glassware technicians.Direct contract performance regarding personnel management, contract preparation and administration in an efficient and professional manner. Ensure the technical and support staff as well as facilities activities meet thesite mission. Ensure that properly trained and experienced personnel are provided to facilitate the needs. Monitor and ensure quality of all facets of facility operations. Monitors performance of employees and conducts periodic performance evaluations; ensure the safety, security and physical environments for all personnel.Investigates personnel problems and provides counseling and disciplinary actions to employees in accordance with company policies and procedures. Manages assigned animal care staff supervisors to ensure the proper inventory, care, feeding and delivery of animals, sanitation of the equipment and facilities, the procurement and storage of supplies and the maintenance of related equipment and facilities. Ensures that detailed, accurate records and files are maintained on regulated species as required by animal welfare, AAALAC, regulations and all research data collection is compliant with client guidelines. Oversees the maintenance of the facility and all animal care equipment through the facility supervisors and animal care staff to ensure proper sanitation and operation.QUALIFICATIONS:Education: Bachelor's degree in Animal Science or related discipline.Experience: Six years of experience in a research animal facility, of which three to five are in a supervisory capacity. Minimum of two years experience in managing a full service animal facility.Certification/Licensure: AALAS certification at the CMAR and LATG are 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.
Project Manager III
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 experience Project Manager III for ourInsourcingSolutionssite located in Atlanta, GA. Indiviaul plans, organizes and directs the activities of the animal husbandry program atcontract site. Manages a staff of area supervisors, veterinary technicians, animal care technicians, cage wash technicians, and glassware technicians.Direct contract performance regarding personnel management, contract preparation and administration in an efficient and professional manner. Ensure the technical and support staff as well as facilities activities meet thesite mission. Ensure that properly trained and experienced personnel are provided to facilitate the needs. Monitor and ensure quality of all facets of facility operations. Monitors performance of employees and conducts periodic performance evaluations; ensure the safety, security and physical environments for all personnel.Investigates personnel problems and provides counseling and disciplinary actions to employees in accordance with company policies and procedures. Manages assigned animal care staff supervisors to ensure the proper inventory, care, feeding and delivery of animals, sanitation of the equipment and facilities, the procurement and storage of supplies and the maintenance of related equipment and facilities. Ensures that detailed, accurate records and files are maintained on regulated species as required by animal welfare, AAALAC, regulations and all research data collection is compliant with client guidelines. Oversees the maintenance of the facility and all animal care equipment through the facility supervisors and animal care staff to ensure proper sanitation and operation.QUALIFICATIONS:Education: Bachelor's degree in Animal Science or related discipline.Experience: Six years of experience in a research animal facility, of which three to five are in a supervisory capacity. Minimum of two years experience in managing a full service animal facility.Certification/Licensure: AALAS certification at the CMAR and LATG are 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.
Necropsy Technician I
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 retrn, we'll help you build a career that you can feel passionate about.Responsibilities We are seeking a Necropsy Technician I for our Safety Assessment site located in Spencerville, OH.The Necropsy Technician will perform basic necropsy laboratory procedures.  During a typical day, you can expect to perform and assist with basic dissection, tissue collection and preservation, fresh tissue trimming, sample collection, etc.  Additionally, you may also receive samples, complete tracking documentation, and prepare pathology materials and data for shipment and archiving.About Safety Assessment BusinessCharles 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. QualificationsThe following are minimum requirements related to the Necropsy Technician I position.High school diploma or General Education Degree (G.E.D.) required.  Associate’s degree (A.A./A.S.) or equivalent in a biological science preferred.1 year of pathology laboratory experience.An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.Must be able to perform effectively as a team member, accurately record data, follow verbal and written instructions, maintain a positive work atmosphere, communicate effectively, and interact in a professional manner with management, coworkers, and sponsors.Must be able to differentiate normal from abnormal tissue.Experience with computer software programs is preferred.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.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.
Necropsy Technician I
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 retrn, we'll help you build a career that you can feel passionate about.Responsibilities We are seeking a Necropsy Technician I for our Safety Assessment site located in Spencerville, OH.The Necropsy Technician will perform basic necropsy laboratory procedures.  During a typical day, you can expect to perform and assist with basic dissection, tissue collection and preservation, fresh tissue trimming, sample collection, etc.  Additionally, you may also receive samples, complete tracking documentation, and prepare pathology materials and data for shipment and archiving.About Safety Assessment BusinessCharles 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. QualificationsThe following are minimum requirements related to the Necropsy Technician I position.High school diploma or General Education Degree (G.E.D.) required.  Associate’s degree (A.A./A.S.) or equivalent in a biological science preferred.1 year of pathology laboratory experience.An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.Must be able to perform effectively as a team member, accurately record data, follow verbal and written instructions, maintain a positive work atmosphere, communicate effectively, and interact in a professional manner with management, coworkers, and sponsors.Must be able to differentiate normal from abnormal tissue.Experience with computer software programs is preferred.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.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.
Scheduling Specialist, Laboratory Sciences
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.BASIC SUMMARY:Perform complex resource planning, coordination and documentation of resource availability for proposed and active studies. Coordinate cross departmental resources and activities and facilitate effective and efficient interdepartmental interaction.ESSENTIAL DUTIES AND RESPONSIBILITIES:Interpret complex study outlines and protocols to assess feasibility, develop timelines and generate study calendars.Establish and prioritize meaningful and clear milestones for all active projects.Assist Client Services, Resources and Study Directors with feasibility and timelines for potential work.Provide leadership and mentoring to schedulers and oversee daily scheduling activities.Identify limiting resources and take action to resolve concerns.Maintain and report on consolidated schedules of all studies.Cost proposals and protocols/amendments.Update key operational dates in various financial/operational systems.Assist in the development, maintenance and communication of departmental BOPs and SOPs.Perform all other related duties as assigned.QualificationsEducation: Bachelor's degree (B.A./B.S.) or equivalent in a scientific or related discipline.Experience: 2 years related experience in a GLP contract research/pharmaceutical setting. 1 year of experience with database administration. Supervisory experience in a GLP environment 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: Comprehensive knowledge of GLP and other federal regulations and guidelines pertaining to preclinical research. Comprehensive knowledge of creating, maintaining and promoting optimal utilization of various database systems. Detail oriented.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. 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.
Scheduling Specialist, Laboratory Sciences
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.BASIC SUMMARY:Perform complex resource planning, coordination and documentation of resource availability for proposed and active studies. Coordinate cross departmental resources and activities and facilitate effective and efficient interdepartmental interaction.ESSENTIAL DUTIES AND RESPONSIBILITIES:Interpret complex study outlines and protocols to assess feasibility, develop timelines and generate study calendars.Establish and prioritize meaningful and clear milestones for all active projects.Assist Client Services, Resources and Study Directors with feasibility and timelines for potential work.Provide leadership and mentoring to schedulers and oversee daily scheduling activities.Identify limiting resources and take action to resolve concerns.Maintain and report on consolidated schedules of all studies.Cost proposals and protocols/amendments.Update key operational dates in various financial/operational systems.Assist in the development, maintenance and communication of departmental BOPs and SOPs.Perform all other related duties as assigned.QualificationsEducation: Bachelor's degree (B.A./B.S.) or equivalent in a scientific or related discipline.Experience: 2 years related experience in a GLP contract research/pharmaceutical setting. 1 year of experience with database administration. Supervisory experience in a GLP environment 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: Comprehensive knowledge of GLP and other federal regulations and guidelines pertaining to preclinical research. Comprehensive knowledge of creating, maintaining and promoting optimal utilization of various database systems. Detail oriented.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. 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.
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