Clinical Trial Coordinator

1 month ago


Vernon BC, Canada LinkedIn - Jobboard Full time

Position : Clinical Trial Coordinator

Location : Vernon Hills, IL

Duration : 12+ Months Contract

Start Time : 8:00 AM

End Time : 5:00 PM

Total Hours/week : 40.00

Experience In Office Documentation Filing Preferred.

  • Strong organizational and interpersonal skills.
  • Practical, detail oriented, flexible and dedicated team player that is capable of working independently.
  • Able to compile brief, coherent, professional documentation and correspondence.
  • Working Knowledge of Microsoft Office.

Experience Preferred

  • data entry, knowledge of administration of clinical trials

Documentation Management

DESCRIPTION OF JOB RESPONSIBILITIES:

  • Scanning, copying, and filing clinical study documentation into eTMF or equivalent documentation tracking and storage system
  • Storage and archiving of study documents for long-term storage Administrative support of clinical trials:
  • Review of initial site regulatory documents
  • Preparation of Investigational Product orders for clinical studies
  • Maintenance of Clinical Database as needed
  • Perform light data entry as needed
  • Interact with clinical vendor site Can be assigned to other equivalent support activities to meet business needs
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