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ERT |
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ePRO Clinical Project SpecialistPosted: November 20, 2009
When getting it done right matters, people count.
ERT does technology with a purpose - to improve and save lives. Our important work sets the industry standard in cardiac safety drug research. Our team provides unparalleled scientific and regulatory leadership to pharmaceutical, biotechnology, contract research organizations (CROs) and medical device companies around the world. Our global clients rely upon our expertise - including our EDC, ePRO, and Consulting Solutions - to flawlessly expedite their clinical research studies.
Based in Bridgewater, NJ the selected candidate will be responsible for assisting the Project Managers throughout the ePRO (electronic Patient Reported Outcomes) study lifecycle. In this role, the Clinical Project Specialist also focuses on each configured system validation and QC, assisting with sending reports to clients as well as administrative duties in support of Project Assurance.
Our qualifications include • College degree (preferably in Health/Life Sciences) • 1-3 years of clinical research/industry experience preferred • Proficiency in Microsoft Word and Excel • Excellent organizational and communication skills; detail oriented • Experience with patient reported outcomes a plus
As an innovative market leader, we provide a competitive salary and comprehensive benefits along with the opportunity to make a difference in the quality of people's lives by the very work you do. Interested and qualified candidates may apply online at: http://www.brightmove.com/ATS/PortalViewRequirement.do?reqGK=43301
www.ertcareers.com
Equal Opportunity Employer
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