Location: Europe, Middle East & Africa-UK-England-Cambridge, Europe, Middle East & Africa, Europe, Middle East & Africa-UK-England-Cambridge - Home Based
Closing Date: 23 Oct 16
Type: Full Time
Salary (£): On Application
Project Manager, Global Clinical Supplies - EMEA PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. ...
Project Manager, Global Clinical Supplies - EMEA PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 46 countries and more than 15,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to help clients and partners bend the cost and time curve of drug development to deliver life-changing therapies that improve health. For more information, visit www.ppdi.com. PPD are currently recruiting for a Project Manager Clinical Supplies to be based within EMEA. The successful candidate will be responsible for providing overall global coordination of the entire clinical supplied lifecycle for the projects assigned. Managing the more complex clinical supplies studies. These studies require primary and or secondary packaging and labelling design, drug projections, drug distribution and returns, drug inventory management, budgeting and developing project specific material for multiple projects at the same time. The clinical supplies department consists of employees located in all regions of the world. This role contributes to the overall strategic objectives of the department by completing assigned objectives in a time and error free manner. Minimum Requirements: Bachelor's degree in a science or related discipline Ability to demonstrate experience in clinical research industry, specifically in the area of Clinical Supplies, Clinical Development, QA/ Regulatory Affairs, Drug Development Ability to demonstrate clinical and internal team interactions Sound understanding of global clinical supply label requirements and regulations Experienced in both protocol interpretation, packaging and labelling design eGMP, GCP, and ICH knowledge experience is preferred
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