Clinical Research Associate

Pleasanton  ‐ Onsite
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Keywords

Description

Roles and Responsibilities:
  • Travels to field sites to monitor studies
  • Review study protocols, reports, and manuscripts
  • Works with Data Management and Biostatistics staff on the design of documents and processes for the collection of study data from participating sites
  • Ensures site compliance with regulations and study protocols
  • Assumes responsibility for training and coordinating certification of study site personnel


Requirements:
  • At least 2-4 years experience as a CRA
  • Diagnostic experience preferred
  • Strong GCP training and overall knowledge
  • Med tech or lab experience is a plus
  • Comfortable monitoring data off of instruments
  • Able to travel 15-30 % during occasional peak periods


To find out more about Real please visit www.realstaffing.com
Start date
10/2013
Duration
18 Months
From
Real Staffing
Published at
09.10.2013
Project ID:
610015
Contract type
Freelance
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