Clinical Trial Associate

South San Francisco  ‐ Onsite
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Keywords

Description

Roles and Responsibilities:
  • Provide logistical support for Study Team
  • Develop, maintain and manage appropriate study documentation
  • Collect, review and approve regulatory documents from clinical sites
  • Initiate, maintain and reconcile Trial Master File
  • Set up and maintain tracking systems and tools and report study metrics to support the clinical study
  • Manage and track clinical and non-clinical supplies


Requirements:
  • 2+ years of industry experience in equivalent role
  • Bachelor's degree or equivalent undergraduate degree required
  • Working knowledge of international regulatory and ICH GCP guidelines
  • Proven organizational skills demonstrated by the ability to understand and prioritize instructions and deliver on time


To find out more about Real please visit www.realstaffing.com
Start date
09/2013
Duration
12 Months
From
Real Staffing
Published at
19.09.2013
Project ID:
601077
Contract type
Freelance
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