Associate Scientist 3

Associate Scientist 3 Req ID #:  75099 Location: 

Boston, MA, US, 02116 For 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. Job Summary We are seeking a Associate Scientist 3for our Discoverysite located inBoston.

Drug Metabolism and Pharmacokinetics group in Boston, MA, is seeking a highly skilled and passionate contractor to support small molecule drug discovery and development. The qualified candidate will work closely with our established in vitro ADME team performing drug transporter, CYP inhibition, and other cell-based assays.

The selected individual will work closely with DMPK team members in Boston to analyze and interpret data which will be presented in a multidisciplinary team environment.

The following are responsibilities related to theAssociate Scientist 3:

Conduct in vitro transporter and CYP inhibition experiments using primary cells and transfected cell lines, etc. Assess drug-drug interaction risk mediated by transporters and metabolic enzymes by evaluating interactions with transporters and drug enzymes Experience with analytical techniques such as LC-MS/MS Perform other duties as assigned

The following are minimum qualifications related to theAssociate Scientist 3position:

Education:Bachelor’s Degree (B.S./B.A) or equivalent in a scientific related discipline.

Experience:Two to four years related laboratory experience, preferably in a pharmaceutical or contract laboratory environment.

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:Demonstrated analytical and problem solving capabilities. Understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and the Good Laboratory Practices (GLPs), as appropriate. Written and verbal communication skills. Ability to organize and prioritize work to meet deadlines under minimal direction. Must be highly motivated, organized with detail oriented, and a good team player.Proficiency in the use of standard software including Microsoft® Excel, Word, Powerpoint, etc. and with standard laboratory calculations. Proficiency in the use of analytical instrumentation software.Experience in cell culture and cell-based assays, and analytic techniques, such as LC-MS/MS.

About Discovery

Discovery 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 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

For more information, please visit www.criver.com.

Nearest Major Market: Boston

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