Demo

Medical Writer III

Katalyst CRO
Antioch, IL Full Time
POSTED ON 4/3/2025
AVAILABLE BEFORE 4/29/2025
Responsibilities

Job Description

Prepare technical documents to support both domestic and international regulatory submissions.

Incorporates text, graphs, charts, tables and statistical analysis. Proofreads, circulates, edits, assembles, inspects and duplicates product submissions. 5 years exp.

Innovative writing with extensive knowledge and understanding of clinical research.

Able to succinctly summarize complex scientific publications and translate science to a lay audience.

Excellent verbal and written communication skills in addition to good interpersonal skills (i.e., build relationships with cross-functional colleagues.

Proficient in the use of Office 365 software such as PPT, Word, Excel, etc.

Proficient in the use of graphics software, including Adobe Illustrator for Medical Writer II.

Preferred For Medical Writer III But Not Required.

Accurate in work, efficient, and contributes to process improvement.

Requirements

PhD in Sciences or Technology, PharmD, or MD for Medical Writer III with 5 years of experience in medical or scientific writing.

Have evidence of publications in peer-reviewed journals as first author and/or has written AMCP dossiers.

Writers with prior experience in AMCP Format and AMCP Dossiers. Certification in oncology.

Individual contributor with cross functional collaboration.

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