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Posted 21 April, 2019

Part Time Administrator (9 month contract)

Charles River Laboratories
Edinburgh, GBR Full Time

Part Time Administrator (9 month contract) Req ID: 43320 Location: Edinburgh, EDH, GB For 70 years, Charles River employees have worked together to...

Part Time Administrator (9 month contract) Req ID: 43320 Location: Edinburgh, EDH, GB 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 Provides office-related administrative support and services. Provides secretarial and clerical support to management and assist with special projects as needed. We are seeking a Part Time Administrator for a 9 Month fixed term contract for our Travel Department site located Tranent. The following are responsibilities related to the Administrator role: + Administrative support to assigned areas on site. + Travel Administrative support to all areas on site. The following are minimum qualifications related to the Administrator position: + Strong organisational skills and attention to detail + The ability to work independently or as part of a team. + Good multi-tasking skills + The ability to prioritise workload and work towards deadlines + Good oral and written communication skills + Work well with staff at all levels and in different departments + Flexible and adaptable to change. + Good knowledge of Microsoft Office, PowerPoint and Word 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. 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 14,000 employees within 80 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. And in 2018, revenue increased by 22% to $2.27 billion from $1.86 billion in 2017. 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 2018.

This listing expired on 21 May. Applications are no longer accepted.

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