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Remote Scientific Technical Writer Jobs in Michigan

Medical Writing Manager

Dearborn, MI ยท Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

Medical Writing Manager

Detroit, MI ยท Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

Medical Writing Manager

Lansing, MI ยท Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

Write and optimize scripts and queries to enhance the functionality of the EcoSys platform ... Bachelor's degree in Computer Science information technology, or a related field. * 4 years of ...

Medical Writing Manager

Ann Arbor, MI ยท Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

Medical Writing Manager

Warren, MI ยท Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

Showing results 21-40

Remote Scientific Technical Writer information

What is a remote scientific technical writer?

A Remote Scientific Technical Writer is a professional who creates clear and accurate documentation related to scientific topics, such as research papers, instruction manuals, protocols, or technical reports, while working from a location outside of a traditional office. They often collaborate with scientists, engineers, and subject matter experts to translate complex scientific information into understandable content for various audiences. Their work is essential in ensuring scientific concepts and research findings are communicated effectively and meet regulatory or publication standards. Working remotely allows them to perform these tasks from anywhere with a reliable internet connection.

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

To thrive as a Remote Scientific Technical Writer, you need a strong background in science or engineering, excellent writing skills, and typically a degree in a relevant field. Familiarity with style guides, reference management software, and document collaboration tools like Microsoft Word and Google Docs is important. Exceptional attention to detail, self-motivation, and the ability to communicate complex information clearly are critical soft skills. These abilities ensure accurate, accessible documentation that supports scientific communication and collaboration in a remote setting.

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

AspectRemote Scientific Technical WriterRemote Scientific Content Developer
CredentialsBachelor's or higher in science/engineering, technical writing certificationsSimilar credentials, often with additional focus on content creation skills
Work EnvironmentRemote, collaborating with scientists and engineersRemote, creating educational or marketing scientific content
Industry UsageUsed in biotech, pharma, research institutionsCommon in science education, marketing, and corporate communications
Search/Comparison IntentUnderstanding technical writing roles in scienceExploring content creation roles in scientific fields

The Remote Scientific Technical Writer and Remote Scientific Content Developer roles share similar credentials and work environments, often within biotech, pharma, or research sectors. While technical writers focus on creating clear, precise documentation, content developers emphasize engaging scientific content for education or marketing. Both roles require scientific knowledge and strong writing skills, but their end goals and content types differ slightly.

How does a remote scientific technical writer typically collaborate with subject matter experts and team members given the remote work setup?

As a Remote Scientific Technical Writer, collaboration with subject matter experts (SMEs) and team members is primarily facilitated through digital communication tools such as email, video conferencing, and project management platforms. Regular virtual meetings and clear documentation processes are essential to clarify technical concepts and ensure accuracy. Writers often coordinate with researchers, scientists, and editors across different time zones, requiring strong organizational skills and proactive communication. Building rapport remotely and maintaining open lines of feedback are key to producing high-quality, precise scientific documentation.
What are the most commonly searched types of Scientific Technical Writer jobs in Michigan? The most popular types of Scientific Technical Writer jobs in Michigan are:
What cities in Michigan are hiring for Remote Scientific Technical Writer jobs? Cities in Michigan with the most Remote Scientific Technical Writer job openings:
Infographic showing various Remote Scientific Technical Writer job openings in Michigan as of August 2026, with employment types broken down into 89% Full Time, 7% Part Time, and 4% Contract. Highlights an 100% Remote job distribution.

Medical Writing Manager

micro1 AI

Dearborn, MI โ€ข Remote

$50 - $80/hr

Part-time

Posted 7 days ago


Job description

Role Title: Medical Writer / Clinical Document Author


Role Type: Contractor


Location: Remote


micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customerโ€™s project focused on developing advanced AI-assisted writing tools for clinical documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required โ€” your domain knowledge is what matters.


Scope of Work

  1. Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.
  2. Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management.
  3. Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.
  4. Trace narrative claims to source recordsโ€”tables, figures, listings, and protocolsโ€”to verify that all assertions are appropriately supported.
  5. Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.
  6. Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.


Preferred Qualifications

  1. Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.
  2. Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.
  3. Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.
  4. Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.
  5. Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.
  6. Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.
  7. Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.


Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents โ€” through your expert input, judgment, and real-world experience.