Charles River Laboratories Senior Research Scientist-Cellular and Molecular Biology in Mattawan, Michigan
Senior Research Scientist-Cellular and Molecular Biology
Req ID #: 80093
Mattawan, MI, US, 49071
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.
We are seeking aSenior Research Scientist for ourCellular and Molecular Biology Team located in Mattawan, MI.
TheSenior Research Scientistin Cellular and Molecular Biology (CMB) is responsible for the performance and development/validation of in vitro, molecular, and/or biochemical techniques, assays and procedures according to applicable Standard Operating Procedures (SOPs), study protocols and/or GxP regulations; the evaluation of new methodologies; and various practical applications, including assisting with study protocol development, recordkeeping, and equipment handling. A Senior Research Scientist represents a key point of contact with sponsors and colleagues through active engagement within the scientific community, including regular meeting attendance along with publishing and presentation of their work with sponsors. The individual in this role works independently, may supervise others, and may function as a Principal Investigator, Project Scientist, Individual Scientist, and/or Study Director.
The following are minimum qualifications related to theSenior Research Scientist position:
• PhD in relevant field and 5-10 years in specialty preferred; or• Master’s degree in relevant field and 7-10 years in specialty preferred; or• Bachelor's degree in relevant field and 10-15 years in specialty; contract research organization experience preferred.• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.• Significant training and expertise in modern cellular biology, molecular biology (including PCR), and/or biochemical techniques and assays.• Outstanding track record in method development.• Proven proficiency in data analysis, research design, troubleshooting, and the evaluation of new technologies and procedures for a cellular and molecular biology lab.• Demonstrated ability to interpret and summarize scientific results in a clear, concise, and accurate manner.• Demonstrated ability to work independently and in a team environment to solve research-related problems and implement new technologies.• Possesses good oral and written communication abilities and strong organizational skills.• Basic familiarity with Microsoft Office Suite.• Computer skills, commensurate with essential Functions, including the ability to learn a validated system.• Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice.• Ability to work under specific time constraints.
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 300 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 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 crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
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