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Remote Technical Writer Jobs in Kenosha, WI (NOW HIRING)

Horizontal Talent

Sr. Medical Writer

Libertyville, IL · On-site +1

$36 - $70/hr

... technical and clinical sources. * Review IFUs, patient materials, training content, risk files ... Experience writing in a medical, pharmaceutical, medical device, clinical research, or related ...

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Remote Technical Writer information

See Kenosha, WI salary details

$13

$37

$64

How much do remote technical writer jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for remote technical writer in Kenosha, WI is $37.74, according to ZipRecruiter salary data. Most workers in this role earn between $27.93 and $45.67 per hour, depending on experience, location, and employer.

What is a remote technical writer?

A Remote Technical Writer is a professional who creates clear, concise documentation such as user manuals, guides, and online help resources for products or services, while working from a location outside of a traditional office. They collaborate with subject matter experts, engineers, or product managers to gather information and translate technical concepts into easily understandable content. Remote Technical Writers use digital communication tools to manage projects, conduct interviews, and deliver documentation, making it possible to work from anywhere with a reliable internet connection.

What does a remote technical writer do?

Remote technical writers create documents that explain complex technical information in simple language that can be understood by anyone. Instead of working in the office, remote technical writers complete their tasks from home or another location outside of the office. As a remote technical writer, your documents may include instruction manuals for power tools, scientific journal articles, and descriptions of computer applications. You research the topic and simplify the industry jargon so that those not in the industry can still understand it. Remote technical writers may be on the staff of a business or writing agency, or they may work as an independent contractor with many different clients.

What key skills and qualifications are needed to thrive as a remote technical writer?

To thrive as a Remote Technical Writer, you need excellent written communication skills, a strong grasp of technical concepts, and relevant qualifications such as a degree in English, communications, or a technical field. Proficiency with documentation tools like Microsoft Word, Adobe FrameMaker, Markdown, and content management systems is typically required. Attention to detail, self-motivation, and the ability to work independently are crucial soft skills for remote collaboration and meeting deadlines. These skills ensure the creation of clear, accurate documentation that supports users and teams across distributed environments.

What are some common challenges faced by remote technical writers, and how can they be addressed?

Remote technical writers often face challenges such as collaborating effectively with subject matter experts across different time zones, staying aligned with rapidly changing project requirements, and maintaining clear communication with development teams. These can be addressed by leveraging collaboration tools (like Slack, Confluence, and Zoom), setting up regular check-ins, and proactively seeking feedback. Building strong relationships with team members and establishing clear documentation processes also help ensure accuracy and consistency in deliverables.

What is the difference between Remote Technical Writer vs Remote Content Writer?

AspectRemote Technical WriterRemote Content Writer
Required CredentialsTechnical degree or background, certifications like STC or SMEWriting or journalism degree, portfolio of diverse content
Work EnvironmentTech companies, engineering firms, software firmsMedia outlets, marketing agencies, online platforms
Employer & Industry UsageHigh in tech, software, engineering sectorsBroad across marketing, media, e-commerce
Search & Comparison IntentTechnical accuracy, documentation skillsCreativity, storytelling, SEO skills

Remote Technical Writers focus on creating detailed technical documentation for technical products, often requiring specialized knowledge and certifications. Remote Content Writers produce a variety of content types for marketing or media purposes, emphasizing creativity and SEO. While both roles involve writing, their industries, skills, and work environments differ significantly.

Are remote technical writers still in demand?

Remote technical writers are still in demand as companies seek clear, concise documentation for products and services. Skills in tools like Markdown, HTML, and content management systems, along with the ability to work independently, are valuable in this field.

How much does a remote technical writer make?

Remote technical writers typically earn between $50,000 and $85,000 annually, depending on experience, industry, and location. Senior or specialized writers with expertise in tools like Markdown or XML can earn higher salaries, especially when working for large organizations or in high-demand fields.
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Remote Technical Writer jobs near you
Infographic showing various Remote Technical Writer job openings in Kenosha, WI as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 9% Part Time, 3% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $78,503 per year, or $37.7 per hour.

Sr. Medical Writer

Horizontal Talent

Libertyville, IL • On-site, Remote

$36 - $70/hr

Full-time

Medical, Dental, Vision, Retirement

Posted 6 days ago

Job description

Join a dynamic regulatory clinical evaluation team supporting the development and life cycle of vascular medical devices. This role is ideal for a detail-oriented medical writer who enjoys turning complex clinical, scientific, and regulatory information into high-quality documentation that supports product submissions and compliance.

Responsibilities
  • Develop and refine clinical evaluation deliverables, including Clinical Evaluation Plans, Clinical Evaluation Reports, SSCPs, regulatory responses, and related documentation.
  • Review and synthesize evidence from clinical studies, published literature, post-market surveillance, risk documentation, and post-market clinical evaluations.
  • Support product applications and submissions by analyzing clinical data and preparing clear, accurate written materials.
  • Collaborate with cross-functional partners across regulatory affairs, quality, clinical affairs, engineering, risk management, medical affairs, sales, marketing, and other stakeholder groups.
  • Maintain familiarity with assigned products and incorporate relevant information from a wide range of technical and clinical sources.
  • Review IFUs, patient materials, training content, risk files, protocols, plans, and reports to help ensure consistency and alignment.
  • Contribute to responses to complex questions from external stakeholders and regulatory bodies.
  • Ensure documentation quality, accuracy, consistency, and compliance with applicable policies, procedures, regulations, and guidance.
Skills
  • Bachelor’s degree or an equivalent combination of education and work experience.
  • 6–8 years of medical writing experience in the medical or pharmaceutical industry, or 8+ years of general technical writing experience.
  • Experience writing in a medical, pharmaceutical, medical device, clinical research, or related environment.
  • Strong written and verbal communication skills with the ability to explain complex information clearly.
  • Excellent analytical skills and the ability to manage multiple priorities and deadlines effectively.
  • Comfort working in collaborative, cross-functional team settings.
  • Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook.
  • Ability to produce accurate work with strong attention to detail and consistency.
Preferred Skills
  • Background in biomedical science, medicine, or another health-related discipline.
  • Prior experience creating Clinical Evaluation Reports and related regulatory documents.
  • Familiarity with clinical study design, clinical study management, quality engineering, or risk management.
  • Experience working with medical device regulatory requirements and guidance, including ISO 13485, ISO 14155, ISO 14791, MEDDEV 2.7.1, MDR, and FDA/EU guidance.
  • Ability to support responses to regulatory inquiries and external questions with sound judgment and professionalism.

Horizontal is committed to fostering an inclusive workplace where diversity, equity, and belonging are valued. We welcome candidates with a wide range of backgrounds, experiences, and perspectives, and we encourage everyone to apply if they meet the core requirements of the role.

By applying for this position, you acknowledge and agree that Horizontal Talent may contact you regarding your application using automated technology, including phone calls, SMS/text messages, or email, which may be delivered by our virtual AI recruiter, Alex.


Please apply through this online posting or by visiting our Job Board at www.horizontaltalent.com/job-board. Applications will be accepted for 4 weeks. For those that join the team, we offer competitive compensation and benefits including medical, dental, vision, and retirement. Check out all we have to offer and how you can become part of the Horizontal Talent Team. The pay range for this role is $36 - $70 per hour based on qualifications and experience.

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