Clinical Studies Specialist

Illinois  ‐ Onsite
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Keywords

Description

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.
Start date
n.a
From
Synectics
Published at
12.11.2015
Project ID:
1018656
Contract type
Freelance
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