Senior Clinical Research Associate

Redwood City  ‐ Onsite
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Keywords

Description

Essential Responsibilities:
  • Independently manage the study start up activities for a multi-center, US based IVD study
  • Responsible for clinical site training and adherence of the site to protocol, according to ICH/GCP guidelines, regulations, and SOPs
  • Mentor and coach junior staff (CTAs)
  • Conduct study qualification visits for the purpose of assessing the site's ability to effectively conduct the trial per SOP and study guidelines
  • Perform relationship management tasks and evaluate CRO performance


Requirements:
  • RN background is strongly preferred; will consider BS/BA in scientific discipline
  • 5+ years of clinical trial monitoring experience
  • OB or diagnostic experience is preferred
  • At least 5 years of medical device clinical trial experience
  • TRAVEL: 40-50 %


To find out more about Real please visit www.realstaffing.com
Start date
11/2013
Duration
12 Months
From
Real Staffing
Published at
06.11.2013
Project ID:
622672
Contract type
Permanent
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