Location: Europe, Middle East & Africa-Italy-Lombardia-Milan
Closing Date: 25 Oct 16
Type: Full Time
Salary (£): On Application
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. ...
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 16,000 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.
Now a great opportunity exists for an experienced professional to join our team at the position of:
Country Approval Associate in Milan on a 12 month FTC
The basic purpose of this position may include, but is not limited to, activities related to obtaining Investigational Product (IP) approval for an individual or group of sites across one or more clinical study including:
Informed consent form review and approval
Regulatory document collection, review and transmittal approval
Adherence to project timelines & expectations
Objectives include the successful coordination of all regulatory and Ethics Committee (EC) tasks required for site IP approval in accordance with FDA Good Clinical Practices, ICH Guidelines and Global Standard Operating Procedures. Represents PPD in the global medical research community and develops collaborative relationships with investigative sites and client company personnel during the start-up of clinical trials
QualificationsEducation and Experience:
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