Clinical Trial Coordinator

millenniumsoft

Behavioral Health Market Context

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Job Description

herent, 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

Qualifications

    Benefits

      Responsibilities

      • Total Hours/week : 40.00
      • 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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