Medical Writer III
ManpowerGroup Global, Inc., Des Plaines, IL, United States
Overview
Job Title:
Medical Writer III
Location:
1300 East Touhy Ave, Des Plaines, IL 60018-3315
Duration:
6 Months
Work Arrangement:
100% Onsite
Pay Range:
$60 - $65 per hour (W2)
We are seeking a
Medical Writer III
to join one of our leading healthcare clients.
Position Summary
The Medical Writer III is responsible for developing high-quality technical and regulatory documents to support domestic and international submissions. This role requires strong attention to detail, the ability to interpret complex data, and expertise in preparing compliant scientific documentation.
Key Responsibilities
Author detailed and accurate technical documents to support regulatory submissions across global markets
Incorporate data, including graphs, charts, tables, and statistical analyses, from approved source materials
Proofread, edit, and compile submission documents to ensure accuracy, consistency, and regulatory compliance
Review and verify documentation for completeness and adherence to submission requirements
Focus Area
Primary focus on
EU IVDR (In Vitro Diagnostic Regulation)
submissions
Qualifications
3–5 years of experience in medical writing or regulatory documentation
Strong expertise in preparing and editing scientific and technical reports
Ability to interpret complex data and present it clearly in structured documents
High attention to detail with strong organizational and communication skills
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Job Title:
Medical Writer III
Location:
1300 East Touhy Ave, Des Plaines, IL 60018-3315
Duration:
6 Months
Work Arrangement:
100% Onsite
Pay Range:
$60 - $65 per hour (W2)
We are seeking a
Medical Writer III
to join one of our leading healthcare clients.
Position Summary
The Medical Writer III is responsible for developing high-quality technical and regulatory documents to support domestic and international submissions. This role requires strong attention to detail, the ability to interpret complex data, and expertise in preparing compliant scientific documentation.
Key Responsibilities
Author detailed and accurate technical documents to support regulatory submissions across global markets
Incorporate data, including graphs, charts, tables, and statistical analyses, from approved source materials
Proofread, edit, and compile submission documents to ensure accuracy, consistency, and regulatory compliance
Review and verify documentation for completeness and adherence to submission requirements
Focus Area
Primary focus on
EU IVDR (In Vitro Diagnostic Regulation)
submissions
Qualifications
3–5 years of experience in medical writing or regulatory documentation
Strong expertise in preparing and editing scientific and technical reports
Ability to interpret complex data and present it clearly in structured documents
High attention to detail with strong organizational and communication skills
#J-18808-Ljbffr