Job Description

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.

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