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Research Assistant II, ADME/DMPK 1

Req ID #:  40836
Location: 

Ashland, OH, US, 44805

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.

 

 

 

We are seeking a Research Assistant I for our safety assessment site located in Ashland, Ohio.

Responsible for the performance of analytical support of animal studies requiring radiochemical analytical techniques in accordance with Good Laboratory Practice Regulations and Standard Operating Procedures with moderate supervision/instruction.  Responsibilities include quantification of various radioactive isotopes in dose preparations, animal samples and extracts, in vitro assays, chromatograhic analyses, whole body autoradiography, and the preparation of relevant study records.

ESSENTIAL DUTIES AND RESPONSIBILITIES:  

  • Perform analysis of moderately complex laboratory assays based on protocols and in compliance with SOPs and GLP regulations.
  • Review documentation of functions performed as part of quality control requirements.
  • Record project data in accordance with GLP regulations.
  • Set up basic laboratory equipment and instrumentation with guidance from senior technical staff.
  • Adhere to current Health and Safety regulations.
  • Perform all other related duties as assigned.

     

    QUALIFICATIONS:

  • Education:  Bachelor’s Degree (B.S./B.A) or equivalent in a scientific related discipline.
  • Experience:  0 to 2 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 prioritize work and meet deadlines. Proficiency in the use of standard software including Microsoft® Excel, Word, Powerpoint, etc. and with standard laboratory calculations.

 

 

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/Vet


Nearest Major Market: Cleveland
Nearest Secondary Market: Mansfield

Job Segment: Toxicology, Biotech, Research Assistant, Pharmaceutical, Science, Research