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Remote Medical Device Technical Writer Jobs in Rochester, NY

micro1 AI

Medical Billing Specialist

Rochester, NY · Remote

$50 - $80/hr

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 ...

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Remote Medical Device Technical Writer information

See Rochester, NY salary details

$13

$38

$57

How much do remote medical device technical writer jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for remote medical device technical writer in Rochester, NY is $38.12, according to ZipRecruiter salary data. Most workers in this role earn between $25.87 and $48.12 per hour, depending on experience, location, and employer.

What is the difference between Remote Medical Device Technical Writer vs Remote Regulatory Affairs Specialist?

AspectRemote Medical Device Technical WriterRemote Regulatory Affairs Specialist
CredentialsTypically requires a degree in life sciences, engineering, or related field; certifications like RMT or technical writing certifications are commonRequires degrees in life sciences, law, or regulatory fields; certifications like RAC are often preferred
Work EnvironmentPrimarily writes and edits technical documents remotely for medical device companiesFocuses on regulatory submissions, compliance, and communication with authorities, often remotely
Industry UsageUsed across medical device companies, biotech, and healthcare tech firmsCommon in medical device, pharmaceutical, and biotech industries

While both roles require knowledge of medical devices and regulatory standards, the Remote Medical Device Technical Writer primarily creates technical documentation, whereas the Remote Regulatory Affairs Specialist manages regulatory compliance and submissions. Both roles often work remotely and require relevant industry experience, but their core responsibilities differ significantly.

What are popular job titles related to Remote Medical Device Technical Writer jobs in Rochester, NY? For Remote Medical Device Technical Writer jobs in Rochester, NY, the most frequently searched job titles are:
What job categories do people searching Remote Medical Device Technical Writer jobs in Rochester, NY look for? The top searched job categories for Remote Medical Device Technical Writer jobs in Rochester, NY are:
What cities near Rochester, NY are hiring for Remote Medical Device Technical Writer jobs? Cities near Rochester, NY with the most Remote Medical Device Technical Writer job openings:
Remote Medical Device Technical Writer jobs near you
Infographic showing various Remote Medical Device Technical Writer job openings in Rochester, NY as of August 2026, with employment types broken down into 64% Full Time, 14% Part Time, and 22% Contract. Highlights an 100% Remote job distribution, with an average salary of $79,292 per year, or $38.1 per hour.

Medical Billing Specialist

micro1 AI

Rochester, NY • Remote

$50 - $80/hr

Part-time

Posted 4 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.

Apply