ZipRecruiter

Log In

2

Remote One Source Medical Solutions Jobs in Georgia

YO AI Labs

Technical Writer - Remote

Atlanta, GA · Remote

$30 - $60/hr

Create and curate source materials such as product specifications, SME notes, regulatory documents ... Define expected solutions, acceptance criteria, and output requirements. * Develop detailed 35 ...

ReSource Pro

Principal AI Solutions Architect

Atlanta, GA · On-site +1

$120K - $205K/yr

ReSource Pro is seeking a Principal AI Solutions Architect, to design, validate, and define AI ... Day 1 * Eligible for all medical, dental, and vision benefits on Day 1 * Remote positions are ...

Fm Talent Source

Data Analyst

Atlanta, GA · On-site +1

F M Talent Source is an enterprise that provides business and workforce solutions to help ... We are seeking a Data Analyst for a full-time contract opportunity with FM Talent Source for one of ...

previous page

Showing results 41-60

All JobsOne Source Medical Solutions JobsRemote One Source Medical Solutions JobsRemote One Source Medical Solutions Jobs in Georgia

Remote One Source Medical Solutions information

What are popular job titles related to Remote One Source Medical Solutions jobs in Georgia?

For Remote One Source Medical Solutions jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Remote One Source Medical Solutions jobs in Georgia look for?

The top searched job categories for Remote One Source Medical Solutions jobs in Georgia are:

What cities in Georgia are hiring for Remote One Source Medical Solutions jobs?

Cities in Georgia with the most Remote One Source Medical Solutions job openings:

Remote One Source Medical Solutions jobs near you

Medical Writer / Clinical Document Author

micro1 AI

Macon, GA • Remote

$50 - $80/hr

Part-time

Re-posted 2 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