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Clinical Trial Associate

New Jersey All, NJ

Posted: 02/04/2019 Job Type: Clinical Job Number: JN -022019-23590
  • Support project teams with preparatory activities for Health Authority inspections and CQA audits
  • Manage documentation associated with clinical trials, both in paper and electronic format
  • Follow records management tasks, policies and procedures protecting record integrity by ensuring full compliance to GCP principles and sponsor SOPs
  • Receive, process and track all clinical project related paper and electronic documents including global study and site documents
  • Review Trial Master File (TMF) binders for completeness and to identify quality/compliance issues
  • Perform quality control checks on TMF site files of paper based studies
  • Bachelors Degree
  • 2 years of CTA experience from a pharma/biotech or CRO organization
  • Understand clinical trial processes and needs
  • Work under pressure and to deadlines
  • Good attention to detail
  • Pro- active, flexible and able to multi-task
  • Work in a team and independently
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