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Remote Medical Technical Writer Jobs in Springfield, MA

micro1 AI

Medical Writing Manager

Hartford, CT · Remote

$50 - $80/hr

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 ...

micro1 AI

Medical Writing Manager

Springfield, MA · Remote

$50 - $80/hr

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 ...

Aflac Incorporated

Claims Technical Lead

Windsor, CT · Remote

$75K - $95K/yr

If the role is remote, there may be occasions that you are requested to come to the office based on ... Excellent Communication skills (verbal, written & presentation). Strong understanding of contracts ...

New

Aflac, Incorporated

Claims Technical Lead

Windsor, CT · Remote

$75K - $95K/yr

If the role is remote, there may be occasions that you are requested to come to the office based on ... written & presentation). • Strong understanding of contracts, plans and products. • Strong ...

New

micro1 AI

Medical Billing Specialist

Hartford, CT · 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 ...

micro1 AI

Medical Billing Specialist

Springfield, MA · 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 Technical Writer information

See Springfield, MA salary details

$14

$38

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

As of Aug 17, 2026, the average hourly pay for remote medical technical writer in Springfield, MA is $38.50, according to ZipRecruiter salary data. Most workers in this role earn between $26.11 and $48.61 per hour, depending on experience, location, and employer.

What is a remote medical technical writer?

A Remote Medical Technical Writer is a professional who creates, edits, and manages medical documents such as clinical study reports, regulatory submissions, and patient information materials, all while working remotely. They translate complex scientific and medical information into clear, accurate, and accessible content for various audiences, including healthcare professionals and regulatory agencies. This role requires strong writing skills, attention to detail, and a solid understanding of medical terminology and regulatory guidelines. Remote medical technical writers often collaborate with researchers, clinicians, and regulatory teams using digital communication tools.

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

To thrive as a Remote Medical Technical Writer, you need a strong background in life sciences or healthcare, excellent writing skills, and familiarity with regulatory or scientific documentation standards. Proficiency in tools like Microsoft Office, referencing software (e.g., EndNote), and document management platforms, as well as certifications like AMWA or EMWA, are often required. Attention to detail, strong organization, and the ability to communicate complex information clearly are critical soft skills. These competencies ensure accuracy, compliance, and effective knowledge transfer in medical communications.

How does a remote medical technical writer typically collaborate with subject matter experts and review teams while working off-site?

Remote Medical Technical Writers frequently collaborate with physicians, researchers, and regulatory professionals via virtual meetings, emails, and document sharing platforms. Effective communication skills and proactive scheduling are essential to clarify complex medical concepts and ensure accuracy in documentation. Writers must be comfortable using collaboration tools like Microsoft Teams or Slack, and version control systems to manage feedback and revisions. Building strong remote relationships and being responsive to queries significantly contribute to a smooth review process and high-quality final deliverables.

What are popular job titles related to Remote Medical Technical Writer jobs in Springfield, MA?

For Remote Medical Technical Writer jobs in Springfield, MA, the most frequently searched job titles are:

What job categories do people searching Remote Medical Technical Writer jobs in Springfield, MA look for?

The top searched job categories for Remote Medical Technical Writer jobs in Springfield, MA are:

What cities near Springfield, MA are hiring for Remote Medical Technical Writer jobs?

Cities near Springfield, MA with the most Remote Medical Technical Writer job openings:

Remote Medical Technical Writer jobs near you
Infographic showing various Remote Medical Technical Writer job openings in Springfield, MA as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 19% Part Time, and 5% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $80,083 per year, or $38.5 per hour.

Medical Writing Manager

micro1 AI

Hartford, CT • Remote

$50 - $80/hr

Part-time

Posted 13 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