For 75 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.
Are you a commercially driven professional with a scientific background in Biology, Pharma, Chemistry, Life Sciences or Environmental Health, seeking a new challenge?
We currently have a challenging open position for a:
Client Coordinator
Department:
The Safety Assessment Client Services department consist of ~130 employees worldwide. The main goal of this department is to understand the client needs and match them with business offerings for a comprehensive range of services for the development of human and veterinary pharmaceuticals, as well as agrochemicals and industrial chemicals.
Team:
The team consists of ~13 employees with various backgrounds in both education (Life Sciences, Biology, Chemistry, Finance, and Hospitality) as in geographical origin (Netherlands, Peru, South Africa, Serbia and more). Within the team there is an open and flexible culture and a pleasant and informal atmosphere.
About the Role:
The Client Coordinator acts as liaison to the Client Managers to provide support to ensure timely, accurate and comprehensive responses to client requests. A full onboarding and trainings program is in place, as well as a nice progression plan within the Client Services department and/or the Charles River organisation.
Key Responsibilities:
- Ensure that all information is complete to qualify client’s requests.
- Support drafting business proposals and adjustments to these business proposals (change orders) based on the client’s requests.
- Follow up with clients to ensure business proposals meet their needs.
- Work with Business Coordination and Specialists, Scientific Operations, Business Development, Project Coordination and Business Finance teams, as required, to ensure that a high-quality customer service is provided.
- Interact with Scientific Operations and Scheduling teams to identify the dates for study initiation and assist with rescheduling studies, as needed.
- Responsible to maintain the Client Service mailbox, i.e. answering questions from clients, operational departments and/or client managers from other sites.
- Update and maintain applicable databases.
- Assist Client Manager with client visits, including giving company tours and presentations.
Qualifications:
- A Bachelor’s or MSc in natural sciences, applying your scientific knowledge in both commercial and scientific contexts.
- Commercial experience, ideally in a scientific field, is a nice to have.
- Availability for 32-40 hours per week. Hybrid working is possible.
The pay range for this position in the Netherlands is 35.000– 45.000 euro on yearly basis. Please note that salaries vary within the range based on
factors including, but not limited to, experience, skills, education, certifications, location and any collective agreements, if
applicable.
Four-year degree required
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.
With over 20,000 employees within 110 facilities in over 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 worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.
At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to fostering a sense of belonging and work daily in this direction.
