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SalaryReq ID: 221050
Location: Edinburgh, GB, EH14 4AP
At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.
Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.
As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe.
Job Summary
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 currently seeking a Scientific Associate for our Biomarker Team located at our site at Clearwater House in Riccarton, Edinburgh.
The larger department of Immunology, Bioanalysis and Biomarkers consists of a dynamic group of approximately 80 researchers that support our clients as they endeavour to bring novel treatments coving a wide range of therapeutic areas to patients. This multifunctional team ensures that clients are provided with accurate and reliable data in order to satisfy the regulatory expectations associated with bringing new treatments to the market. This is accomplished using a wide variety of scientific techniques across the fields of Immunochemistry, Immunology, Cell Based Assays and Molecular Biology.
As part of the Biomarker team, the successful applicant will be involved in the development, validation, and implementation of immunoassays to support Biomarker assessments including those considered Safety; Pharmacodynamic; Surrogate; Predictive/Prognostic; Monitoring and Susceptibility.
The larger department of Immunology, Bioanalysis and Biomarkers consists of a dynamic group of approximately 80 researchers that support our clients as they endeavour to bring novel treatments coving a wide range of therapeutic areas to patients. This multifunctional team ensures that clients are provided with accurate and reliable data in order to satisfy the regulatory expectations associated with bringing new treatments to the market. This is accomplished using a wide variety of scientific techniques across the fields of Immunochemistry, Immunology, Cell Based Assays and Molecular Biology.
As part of the Biomarker team, the successful applicant will be involved in the development, validation, and implementation of immunoassays to support Biomarker assessments including those considered Safety; Pharmacodynamic; Surrogate; Predictive/Prognostic; Monitoring and Susceptibility.
Key responsibilities include, but are not limited to:
- Processing of samples
- Operation of state-of-the-art analytical equipment
- Recording and reporting of data.
Profile and Requirements
Profile and Requirements
We are looking for applicants with excellent organisational skills with an eye for detail and quality. In addition to the following skills and experience, the candidate should have a BSc or MSc degree in a relevant discipline with good understanding of Immunology and Cell biology or drug development.
Specific criteria that you are required to meet include:
Specific criteria that you are required to meet include:
- Strong team player with good communication skills
- Interest in working with sophisticated laboratory equipment
- Understanding of core laboratory skills and techniques
- Ability to perform well and thrive in a high-pressure environment
- Basic understanding of GLP and GCP
The starting salary for this role is £26,244.91 and this role closes Tuesday, 23 January 2024.
Following initial training and onboarding at our site based in Elphinstone, Tranent, the successful candidate will be based at our site in Clearwater House, Riccarton.
Due to high volume of applications we are receiving if you have not heard anything from Charles River Laboratories Edinburgh regarding the next steps of our recruitment process within 3 weeks of the closing date then please conclude you have been unsuccessful.
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.
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.
With over 20,000 employees within 110 facilities in 20 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.
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 86% of the drugs approved by the FDA in 2021.
At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.
For more information, please visit www.criver.com.
