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Remote International Medical Data Entry Jobs in Springfield, MA

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... source data. * Exceptional written and verbal communication skills, especially in providing ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... source data. * Exceptional written and verbal communication skills, especially in providing ...

Chronic Practice Liaison

Hartford, CT · Remote

$66K - $88K/yr

Ability to work with Microsoft Windows-based programs, and acceptable data entry skills required ... Primarily remote with virtual engagement Preferred Qualifications & Interests (PQIs) * Bachelor ...

Chronic Practice Liaison

Hartford, CT · Remote

$66K - $88K/yr

Ability to work with Microsoft Windows-based programs, and acceptable data entry skills required ... Primarily remote with virtual engagement Preferred Qualifications & Interests (PQIs) * Bachelor ...

Review medical history, symptoms, and treatment concerns shared through Dutch's digital platform ... If you would like more information about how your data is processed, please contact us. apply for ...

Showing results 21-40

Remote International Medical Data Entry information

See Springfield, MA salary details

$12

$17

$22

How much do remote international medical data entry jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for remote international medical data entry in Springfield, MA is $17.86, according to ZipRecruiter salary data. Most workers in this role earn between $16.06 and $19.18 per hour, depending on experience, location, and employer.

What is the difference between Remote International Medical Data Entry vs Remote Medical Transcriptionist?

AspectRemote International Medical Data EntryRemote Medical Transcriptionist
CredentialsBasic medical data entry skills, sometimes certification in medical terminologyMedical transcription certification often preferred, knowledge of medical terminology
Work EnvironmentRemote, computer-based, often international clientsRemote, audio-to-text transcription, healthcare settings
Employer & IndustryHospitals, clinics, medical data companies worldwideHealthcare providers, transcription services, medical offices
Search & Comparison IntentUnderstanding data entry roles in healthcareTranscription of medical audio files

Remote International Medical Data Entry involves inputting medical information into databases, often for international clients, requiring basic medical terminology knowledge. Remote Medical Transcriptionist focuses on converting audio recordings into written reports, emphasizing transcription skills and medical terminology. Both roles are remote healthcare jobs but differ in tasks and skill sets.

What are popular job titles related to Remote International Medical Data Entry jobs in Springfield, MA? For Remote International Medical Data Entry jobs in Springfield, MA, the most frequently searched job titles are:
What job categories do people searching Remote International Medical Data Entry jobs in Springfield, MA look for? The top searched job categories for Remote International Medical Data Entry jobs in Springfield, MA are:
What cities near Springfield, MA are hiring for Remote International Medical Data Entry jobs? Cities near Springfield, MA with the most Remote International Medical Data Entry job openings:

Medical Billing Specialist

micro1 AI

Springfield, MA • Remote

$50 - $80/hr

Part-time

Posted 5 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.