Location: USA Remote – any time zone
Hours: 20 to 30 hours per week
Comments:
Nature of Role:
• Will work with domestic documents so must have familiarity with authoring documents, scientific publications, data outputs, and data repository to pull documents from.
• Will be creating legend from graphs to text.
• Outputs into templates & creates summary.
• Must have MS Office Suite knowledge specifically Word and PPT Experience in Cardiology is a plus, however 2-3 years of experience must come from Life-Sciences, Medical Device, Pharma, with Regulatory Reports knowledge, and Graphs knowledge.
What You’ll Work On
• Prepare technical documents to support both domestic and international clinical studies.
• Author annual progress reports on clinical trials and studies in Client Structural Heart’s transcatheter edge-to-edge repair portfolio.
• Collaborate with clinical and biometrics to ensure proper content is included in documents.
• Incorporate statistical outputs, text, graphs, charts, and tables into clinical reports or publication projects with high attention to detail in a clear and accurate manner.
• Construct and draft publication projects (abstracts, presentations, manuscripts) for peer-review submissions.
• Review and proofread all types of materials for accuracy, consistency, and clarity.
• Review, circulate, edit, assemble, and inspect submissions.
• Communicate deliverables needed and writing process to team members.
• Utilize templates and format/style guidelines necessary for document type.
• Incorporates text, graphs, charts, tables and statistical analysis.
• Proofreads, circulates, edits, assembles, inspects and duplicates product submissions.
• 3-5 years exp
Qualifications
• 1-3+ years of experience as a medical or technical writer (publications or regulatory).
• Bachelor’s Degree in relevant technical discipline, including biology, engineering, physiology, data science, statistics, or similar.
• Masters Degree preferred.
• Exceptional writing and proofreading skills, experience with AMA Manual of Style.
• Multitasks, prioritizes, and meets deadlines in a timely manner.
• Strong organizational and follow-up skills, as well as attention to detail
Job Type: Contract
Pay: $42.00 – $44.00 per hour
Expected hours: 40 per week
Benefits:
• Flexible schedule
• Health insurance
• Life insurance
• Paid time off
Schedule:
• 8 hour shift
• Day shift
• Monday to Friday
Education:
• Master’s (Preferred)
Experience:
• Publications writing: 5 years (Preferred)
• Pharma or medical device industry: 5 years (Preferred)
• Author annual progress reports on clinical trials: 5 years (Preferred)
• create documents for clinical studies: 5 years (Preferred)
• scientific publications,: 5 years (Preferred)
• inspects and duplicates product submissions.: 5 years (Preferred)
Work Location: Remote
Location: , ,
Job Posting Language: en
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