Data Entry Clerk

Mindlance; Saint Joseph (MO); On-site; USD 35,000 - 50,000; Full time

Job summary

A national recruiting company is looking for a detail-oriented data entry professional to manage investigator site information in the Clinical Trial Management System. Applicants should have proficiency in Microsoft Office applications and an Associates Degree in Life Science is preferred. Responsibilities include data entry from Case Report Forms and ensuring quality checks on documents. This role is crucial to maintaining accurate and efficient data management for clinical trials.

Qualifications

• Proficient in Microsoft programs including Excel, Word, Visio, and PowerPoint.
• Strong attention to detail required for data quality checks.
• Experience with Clinical Trial Management Systems (CTMS) is beneficial.

Responsibilities

• Enter accurate investigator site information into the CTMS.
• Distribute documents into the central file and prepare relevant documents.
• Perform quality checks and audits on data entry and various media.

Skills

Microsoft Excel

Microsoft Word

Attention to detail

Teleform Designer

Education

Associates Degree in Life Science

Job description

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at http://www.mindlance.com.

Job Description

• Responsible for entering accurate investigator site information into the 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

• Microsoft programs (Excel, Word, Visio, PowerPoint, Adobe Acrobat and Outlook).
• Attention to detail is must.
• Associates Degree in Life Science preferred.

Additional Information

All your information will be kept confidential according to EEO guidelines.