Clinical Trial Coordinator
Clinical Trial Coordinator
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
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 longterm 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
Required Experience:
IC
Employment Type
Full Time
