Job Description
Duties:Responsible for entering accurate information investigator site information to Clinical Trial Management System (CTMS) from the pre-designed template.
Distribute documents into central file
Perform quality check and audits from various media types back to source
Prepare and test raw data for data entry in Clinical Trial Master System software
Create data entry relevant documents required for data entry
Enter data from Case Report Forms into Clinical Trial Master System software
Serve as specialized user for Teleform Designer and Clinical Trial Master System software.
Case Report Form creation using Teleform Software.
Assist in the creation of annotated Case Report Forms
Preparing and modifying a broad scope of confidential and complex study documents.
Perform quality check procedures
Qualifications
Skills:Microsoft programs (Excel, Word, Visio, PowerPoint, Adobe Acrobat and Outlook)
Attention to detail is must
Education:
Associates Degree in Life Science preferred
Additional Information
All your information will be kept confidential according to EEO guidelines.