Senior Research Scientist

Req ID #:  108651
Location: 

Cleveland, OH, US, 44128

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 Senior Research Scientist for our Safety Assessment Group site located Cleveland, OH.

 

The following are responsibilities related to the Senior Research Scientist:  Serve as a scientist in the conduct of assigned nonclinical research studies at all levels of complexity, to include study management, interpretation and reporting of study data, and assuring the regulatory compliance of these projects, as appropriate. Additional responsibilities include serving as a primary scientific contact for key clients and the on-site support of their programs, as well as the support of specialty studies.

 

•    Function independently as a study director in the direction and execution of assigned studies, in compliance with Good Laboratory Practice (GLP) regulations as they apply to the conduct of nonclinical research.
•    Participate in the proposal management and bid development process, serving as a key scientific contact for new business generated from established business relationships.  
•    Participate in and coordinate all phases of the study planning process with appropriate departments.
•    Generate high-quality protocols, amendments, and reports appropriate for assigned studies.
•    Review, interpret, integrate, and present data on assigned studies with minimal assistance.
•    Function independently as contact for the planning and execution of sponsor interaction related to assigned studies, including proposal management and study scheduling, conduct and reporting.
•    Assist in the oversight of the laboratory and mentor technical staff in areas such as protocol interpretation, method development and refinement, study-related problem resolution, and technique validation.  Provide scientific expertise in study conduct, design, and interpretation.
•    Attend scientific meetings, conferences, and training courses to enhance job and professional skills. Present abstracts/posters at national meetings, when appropriate, to maintain a scientific presence and visibility in areas of individual expertise.
•    Recommend and implement techniques to improve productivity, increase efficiencies, cut costs, take advantage of opportunities, and maintain state-of-the-art practices.
•    Perform testing facility management duties for the site as delegated by senior management.
•    Perform all other related duties as assigned.

 

The following are minimum qualifications related to the Senior Research Scientist position:

•    Education:  Ph.D. in Cell Biology, Biochemistry, Toxicology or a related scientific discipline required.
•    Experience:  Minimum of 9 to 12 years related experience in a contract research organization (CRO), academic, biotechnology or pharmaceutical environment.  Previous experience developing and interpreting the results of complex in vitro toxicology assays required.  Experience        working to GLP standards required.  Experience working with novel alternative methods for in vitro toxicology assessment preferred.

 

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 14,000 employees within 80 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 2018, revenue increased by 22% to $2.27 billion from $1.86 billion in 2017.

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 2018.

 

Equal Employment Opportunity 

 

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet

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Nearest Major Market: Cleveland

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