Charles River Laboratories
Principal Research Scientist - Laboratory Sciences
Charles River Laboratories, Reno, Nevada, United States, 89550
Principal Research Scientist - Laboratory Sciences
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Principal Research Scientist - Laboratory Sciences
role at
Charles River Laboratories
Overview 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, dedicated to continuous learning and improvement, and will be empowered 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, helping bring 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, you will be the difference every day for patients across the globe.
Responsibilities
Developing and validating ligand binding assays in support of Pharmacokinetic/Toxicokinetic, Immunogenicity and biomarker studies.
Utilizing a variety of platforms (ELISA, ECL, Luminex, Gyros, etc.) and providing recommendations to clients during study planning and assay design.
Acting as a lead scientist in the planning and execution of assigned studies.
Interpreting data for studies, providing scientific rigor, integrating supporting data, and preparing high-quality reports.
Mentoring junior scientists and providing scientific direction for complex studies.
Participating in the bioanalytical scientific community internally and externally by engaging in working groups and committees.
Recommending and implementing scientific platforms and technologies based on industry direction.
Reviewing papers, working on publications, and developing presentations to support growth in bioanalytical sciences.
Qualifications
Experience developing and validating ligand binding assays for bioanalysis, immunogenicity testing and biomarker measurement in non-clinical and clinical studies.
Experience in the contract research or pharmaceutical industry conducting scientific research.
Experience in a GLP environment; assay development experience; experience with project management and drug development.
Education
PhD and 6 years of experience in bioanalytical sciences OR
Master’s degree and 8 years of experience in bioanalytical sciences OR
Bachelor’s degree and 10 years of experience in bioanalytical sciences
Compensation Note: The pay range for this position is $130,000 - $135,000 annually. 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 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. We also provide a suite of products and services to support clinical laboratory testing needs and manufacturing activities. Our broad portfolio enables a flexible drug development model, reducing costs and increasing productivity and speed to market.
With over 17,000 employees within 90 facilities in 20 countries, we coordinate worldwide resources and apply multidisciplinary perspectives to resolve challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies, hospitals and academic institutions. In 2019, revenue was $2.62 billion. Our mission is to improve the health and well-being of people worldwide, and 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 need special assistance or an accommodation due to a disability to complete any forms or participate in the resume submission process, please contact a member of our Human Resources team by emailing crrecruitment_US@crl.com. This contact is for accommodation requests and cannot be used to inquire about application status. For more information, please visit www.criver.com.
229528
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Principal Research Scientist - Laboratory Sciences
role at
Charles River Laboratories
Overview 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, dedicated to continuous learning and improvement, and will be empowered 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, helping bring 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, you will be the difference every day for patients across the globe.
Responsibilities
Developing and validating ligand binding assays in support of Pharmacokinetic/Toxicokinetic, Immunogenicity and biomarker studies.
Utilizing a variety of platforms (ELISA, ECL, Luminex, Gyros, etc.) and providing recommendations to clients during study planning and assay design.
Acting as a lead scientist in the planning and execution of assigned studies.
Interpreting data for studies, providing scientific rigor, integrating supporting data, and preparing high-quality reports.
Mentoring junior scientists and providing scientific direction for complex studies.
Participating in the bioanalytical scientific community internally and externally by engaging in working groups and committees.
Recommending and implementing scientific platforms and technologies based on industry direction.
Reviewing papers, working on publications, and developing presentations to support growth in bioanalytical sciences.
Qualifications
Experience developing and validating ligand binding assays for bioanalysis, immunogenicity testing and biomarker measurement in non-clinical and clinical studies.
Experience in the contract research or pharmaceutical industry conducting scientific research.
Experience in a GLP environment; assay development experience; experience with project management and drug development.
Education
PhD and 6 years of experience in bioanalytical sciences OR
Master’s degree and 8 years of experience in bioanalytical sciences OR
Bachelor’s degree and 10 years of experience in bioanalytical sciences
Compensation Note: The pay range for this position is $130,000 - $135,000 annually. 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 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. We also provide a suite of products and services to support clinical laboratory testing needs and manufacturing activities. Our broad portfolio enables a flexible drug development model, reducing costs and increasing productivity and speed to market.
With over 17,000 employees within 90 facilities in 20 countries, we coordinate worldwide resources and apply multidisciplinary perspectives to resolve challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies, hospitals and academic institutions. In 2019, revenue was $2.62 billion. Our mission is to improve the health and well-being of people worldwide, and 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 need special assistance or an accommodation due to a disability to complete any forms or participate in the resume submission process, please contact a member of our Human Resources team by emailing crrecruitment_US@crl.com. This contact is for accommodation requests and cannot be used to inquire about application status. For more information, please visit www.criver.com.
229528
#J-18808-Ljbffr