Clinical Studies Specialist

Job type:
on-site
Start:
n.a
Duration:
n.a
From:
Synectics
Place:
Illinois
Date:
11/12/2015
Country:
flag_no USA
project ID:
1018656

Warning
This project is archived and not active any more.
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Summary
  • Ensure documents are compliant with SOPs and regulatory requirements.
  • Review essential/critical documents for completeness and accuracy.
SKILLS:

Qualifications
  • Pharma experience or professional equivalent.
  • Ability to manage clinical documents for multi-site studies.
  • Ability to prioritize multiple tasks and/or projects with limited supervision.
  • Ideal candidates will possess strong organizational capabilities and strong interpersonal skills, excellent written and verbal skills.