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Charles River Laboratories: Research Assistant 2 (Pharmacology & Discovery Srvcs. )

Charles River Laboratories

This is a Full-time position in Ashland, OH posted October 7, 2021.

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 Research Assistant 2 for our Safety Assessment group site located in Ashland Ohio.

Perform moderately complex research, analysis and laboratory work in collaboration with departmental staff.

Responsibilities:Perform duties to support Safety Pharmacology study designs to include room set up and test system preparation for data collection with guidance/oversight from senior staff.Perform analysis of moderately complex physiological data based on protocols and in compliance with SOPs and GLP regulations.Support Global Safety Pharmacology CRL sites for analysis and measurement of physiological data.Review documentation of functions performed as part of quality control requirements.Record study data in accordance with GLP regulations.Adhere to current Health and Safety regulations.Perform all other related duties as assigned.

Qualifications:Bachelor’s Degree (B.S/B.

A.) or equivalent in a scientific related discipline.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.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 AssessmentCharles 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.