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Research Associate I Clinical Pathology 1

Req ID #:  44545
Location: 

Ashland, OH, US

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 an Research Associate I for our Safety Assessment site located in Ashland, Ohio.

Assist scientific staff by working under general guidance/supervision on basic scientific support, report development, regulatory compliance, and research.

ESSENTIAL DUTIES AND RESPONSIBILITIES: 

 

  • Review protocols and amendments if applicable.
  • Review study file for accuracy of scope of work prior to study initiation.
  • Provide input to supervisors on workload prioritization.
  • Prepare basic tables for department metric reports.
  • Attend weekly study meetings.
  • Conduct basic literature searches.
  • Provide quality control review of processing and shipping documentation as needed.
  • Coordinate the acquisition of materials from internal departments to ensure the proper handling of unique study protocols.
  • Perform all other related duties as assigned.

    QUALIFICATIONS:

  • Education:   Bachelor’s degree (B.S./B.A.) or equivalent in biology, zoology, chemistry, pathology or related field preferred.
  • Experience:  0-2 years of relevant experience. Experience in the biomedical research industry desired.  Technical laboratory experience is preferred.
  • Proficient in basic technical skills and the operation of data collection equipment.
  • Basic understanding of study design and protocols; able to read basic study protocols and extract pertinent information.

Must be able to perform effectively as a team member, accurately record data, follow verbal and written instructions, communicate effectively, and interact in a professional manner with management, coworkers, and sponsors.

 

 

 

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 Associate, Pharmaceutical, Science, Research