Research Associate 1

1 month ago

Tranent, United Kingdom Charles River Laboratories Full time

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.

At our world class facility in Elphinstone, Tranent (close to Edinburgh), our Pathology Department currently has an exciting career opportunity for a **Research Associate.**

The Pathology Department provides support to the Pharmaceutical, Biotechnology, Veterinary Medicine sectors by interpreting the pathology data from Regulatory Safety Assessment, Target Animal Safety and Discovery studies in a variety of test species.

Key Responsibilities:

- Assist in the production of all pathology reports and data;
- Respond to QAU audits;
- Liaise with Clients;
- Assist with archiving of pathology data;
- Conduct Historical Control Data searches;
- Prepare electronic LIMS data Excel or Word tables for Pathologist assessment;
- Assist in scheduling Pathologist workloads

Applicants should have:_ _
- Minimum of 5 Higher grades/3 A levels including Biology
- Strong PC skills with knowledge of all Microsoft Packages
- A good work ethic with the ability to work to tight timescales
- Knowledge of GLP and/or GMP preferred

**Salary**: £22,563.88 per annum.

Closing Date: 06 April 2023

**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.

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