Scientific Associate 1

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**:
The Bioscience Division provides support to the pharmaceutical, veterinary pharmaceutical and chemical/agrochemical industries by evaluating the metabolism, distribution and elimination (ADME) of new chemical and biological entities both in vitro and in vivo in a variety of test systems.
- Accurate and detailed documentation of activities
- Use of general lab equipment including LSC, HPLC, TLC.
- Generation of critical electronic data
- Assisting with the preparation of data and reports for issue to clients
- Engagement in staff training and development programs
- Supervision of staff (where required)

Applicants should be educated to degree level ideally in a chemistry or life sciences (with a chemistry component) related discipline. Relevant laboratory experience in the conduct of regulatory studies would be advantageous, however, full training will be provided.

Specific criteria that you are required to meet include:

- Relevant qualifications, specifically a minimum of a scientific degree in a relevant discipline.
- A strong eye for detail and excellent documentation skills.
- Excellent communication, organisation and time management skills as well as an ability to work flexibly and to tight deadlines
- A working knowledge of Microsoft Office or scheduling software would be beneficial.

Closing date: 26 August 2025

Salary for this position is: £27,951.22 per annum.

**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 300 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.

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 2019.

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