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Remote Development Writer Jobs in Virginia (NOW HIRING)

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... development. * Apply expert judgment to assess whether AI-generated content fulfills clinical ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... development. * Apply expert judgment to assess whether AI-generated content fulfills clinical ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... development. * Apply expert judgment to assess whether AI-generated content fulfills clinical ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... development. * Apply expert judgment to assess whether AI-generated content fulfills clinical ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... development. * Apply expert judgment to assess whether AI-generated content fulfills clinical ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... development. * Apply expert judgment to assess whether AI-generated content fulfills clinical ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... development. * Apply expert judgment to assess whether AI-generated content fulfills clinical ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... development. * Apply expert judgment to assess whether AI-generated content fulfills clinical ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... development. * Apply expert judgment to assess whether AI-generated content fulfills clinical ...

Showing results 21-40

Remote Development Writer information

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

AspectRemote Development WriterRemote Content Writer
Required CredentialsTechnical writing skills, familiarity with development topics, possibly coding knowledgeStrong writing skills, general research ability, SEO knowledge
Work EnvironmentTypically collaborates with developers, tech teams, and product managersWorks with marketing teams, editors, and content strategists
Employer & Industry UsageTech companies, software firms, development agenciesMedia outlets, marketing agencies, corporate blogs
Search & Comparison IntentUnderstanding technical writing roles in developmentExploring general content creation roles

Remote Development Writers focus on creating technical documentation, tutorials, and guides related to software development, requiring technical expertise. Remote Content Writers produce a broader range of content, including blogs, articles, and marketing materials, with less technical specialization. Both roles are remote, but their target industries and skill sets differ significantly.

What are the most commonly searched types of Development Writer jobs in Virginia?

The most popular types of Development Writer jobs in Virginia are:

What cities in Virginia are hiring for Remote Development Writer jobs?

Cities in Virginia with the most Remote Development Writer job openings:

Medical Writer / Clinical Document Author

micro1 AI

Virginia Beach, VA • Remote

$50 - $80/hr

Part-time

Posted 12 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 customer’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 — 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 records—tables, figures, listings, and protocols—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 — through your expert input, judgment, and real-world experience.