Medical Writer (Des Plaines)
KPG99 INC, Des Plaines, IL, United States
Title:
Medical Writer
Location: Des Plaines, IL – Onsite
Duration: 12 Months Contract.
Interview Mode : Phone + Video
Responsibilities:
Author technical documents with a high level of detail and precision to support domestic and international regulatory submissions.
Incorporate graphs, charts, tables, and statistical analyses from approved source files.
Proofread, edit, circulate, assemble, and inspect submission documents for accuracy and compliance.
5 days onsite (Des Plaines currently)
Must have a strong understanding of EU IVDR and/or MDR (Medical Device Regulation)
Must have a strong understanding of how to complete submissions following EU and product completion submissions. Writing technical documents for those submissions.
Will be working within the Molecular Diagnostics division and within In Vitro area.
Microsoft WORD and working with Abode Acrobat (everything rendered in Adobe and has to render and modify images, etc.)
Soft Skills: People who can take feedback , flexibility and being able to shift priorities if a specific chapter needs to take precedence, time management
Desired Skillset:
3- 5 years of experience in medical writing or regulatory documentation.
Strong skills in preparing and editing scientific reports.
Ability to work with complex data and present it clearly in technical documents.
Medical Writer
Location: Des Plaines, IL – Onsite
Duration: 12 Months Contract.
Interview Mode : Phone + Video
Responsibilities:
Author technical documents with a high level of detail and precision to support domestic and international regulatory submissions.
Incorporate graphs, charts, tables, and statistical analyses from approved source files.
Proofread, edit, circulate, assemble, and inspect submission documents for accuracy and compliance.
5 days onsite (Des Plaines currently)
Must have a strong understanding of EU IVDR and/or MDR (Medical Device Regulation)
Must have a strong understanding of how to complete submissions following EU and product completion submissions. Writing technical documents for those submissions.
Will be working within the Molecular Diagnostics division and within In Vitro area.
Microsoft WORD and working with Abode Acrobat (everything rendered in Adobe and has to render and modify images, etc.)
Soft Skills: People who can take feedback , flexibility and being able to shift priorities if a specific chapter needs to take precedence, time management
Desired Skillset:
3- 5 years of experience in medical writing or regulatory documentation.
Strong skills in preparing and editing scientific reports.
Ability to work with complex data and present it clearly in technical documents.