Project Scheduler

2 weeks ago

Tranent, United Kingdom Charles River Laboratories Full time

**Req ID**:220111**Location**:Tranent, GB, EH33 2NE- 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 looking to recruit a Project Scheduler for our
**Toxicology Administration & Reporting** department located in
**Elphinstone, Tranent**.
Collaborating with various key stakeholders including study management, client managers and support staff, you will review and understand specific study requirements in order to proactively schedule projects for the company and maintain the site scheduling tool.
In addition, you will prepare reports from these databases for use both globally and for the site Test Facility Management and Client Service managers.

**About Toxicology Administration & Reporting**
The Toxicology Administration and Reporting department provides an efficient administrative support to study management in the running of safety assessment studies. We use various databases to ensure the effective planning, scheduling and reporting of the studies, to the standards required by the Company, its clients and international regulatory authorities.
The following are minimum requirements related to the
**Project Scheduler** position.
- High degree of IT literacy, in particular, extensive experience in use of Microsoft Excel and database management.
- Excellent attention to detail, verbal and written communication skills.
- Ability to remain composed when faced with unplanned changes.
- Determination to complete jobs to tight timescales whilst maintaining a high standard.
- Ability to confidently interact with people at all levels.
- Flexible approach to working in an environment where meeting clients’ deadlines is critical.
- Commitment to the importance of quality is essential for this position
- Experience in calendar management for multiple stakeholders
- Knowledge of Good Laboratory Practice is an advantage.

Starting salary for this position is £26,244. with opportunity for progression and salary increments at regular intervals.

**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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