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
 
DESCRIPTION OF JOB RESPONSIBILITIES:
Documentation Management:
- 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