Clinical Data Specialist

Added
2 minutes ago
Type
Full time
Salary
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Related skills

ms office quality assurance gcp data entry edc

πŸ“‹ Description

  • Attend study setup meetings to determine QC criteria and timelines.
  • Review source documents to ensure forms align with CRFs and protocols.
  • Ensure QC reviews are completed per study timelines.
  • Review data for GCP/FDA compliance and document deviations.
  • Perform data entry and verification for EDCs.
  • Archive source documentation including CRFs.

🎯 Requirements

  • High School Diploma or GED; internal Celerion experience preferred
  • 1-2 years industry experience preferred
  • Previous QC or data entry experience preferred
  • Medical terminology training preferred
  • Excellent oral and written communication
  • Proficient in MS Office applications

🎁 Benefits

  • Equal Opportunity Employer
  • Celerion values: Integrity, Trust, Teamwork, Respect
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