Location: Europe, Middle East & Africa-Greece-Attica-Athens
Closing Date: 24 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 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 was ranked one of the world’s best contract research organizations (CROs) in the CenterWatch 2015 Global Site Survey and PPD was recognized as one of the leading businesses for employee learning and development.
We have an opportunity for you - join our team of global professionals!
Currently we have an exciting career opportunity within our Clinical Department in Athens for:
Clinical Research Associate
The successful candidate will be primarily tasked to set up and monitor clinical trials conducted as part of international projects. He/She will need to perform and coordinate all aspects of the clinical monitoring process from "start up" to "close out" of the trial. The Clinical Research Associate will be also responsible for determining protocol and regulatory compliance on the sites; and for thriving in multi-national project teams in order to deliver exemplary levels of customer service.
QualificationsQualifications: The opportunity is suitable for a professional with a life-science degree and proven experience within a CRO, pharmaceutical or biotech company on a similar position. We’re specifically looking for a qualified professional with 2-3 years of experience in interventional studies.
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