Clinical Research Associate - Pleasanton, med device/diagnostic

Pleasanton  ‐ Onsite
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Keywords

Description

Roles:
  • Travels to field sites to monitor studies
  • Collects and maintains legal and regulatory documentation, as applicable
  • Ensures site compliance with regulations and study protocol
  • Manages material logistics for the studies
  • Works with Data Management and Biostatistics staff on the design of documents and processes for the collection of study data from participating sites
  • Maintains a high level of professional expertise through familiarity with scientific literature, Company product portfolio, and competitve environments


Requirements:
  • Bachelors degree in a scientific discipline or equivalent; MS or PhD preferred
  • 6+ years of Clinical Research Associate experience
  • Travel: up to 30%
  • Medical device or diagnostic clinical trial experience
  • Working knowledge of ICH GCP guidelines


To find out more about Real please visit www.realstaffing.com
Start date
11/2013
Duration
18 months
From
Real Staffing
Published at
14.11.2013
Project ID:
626733
Contract type
Freelance
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