Clinical Trial Coordinator

Pay Rate: 14 - 18$/hr

• 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.

• 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.

• data entry, knowledge of administration of clinical trials

• 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