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Medical Content Reviewer Jobs in Raleigh, NC (NOW HIRING)

micro1 AI

Medical Writing Manager

Raleigh, NC · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... Apply expert judgment to assess whether AI-generated content fulfills clinical template and ...

micro1 AI

Medical Billing Specialist

Durham, NC · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... Apply expert judgment to assess whether AI-generated content fulfills clinical template and ...

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How much do medical content reviewer jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for medical content reviewer in Raleigh, NC is $40.88, according to ZipRecruiter salary data. Most workers in this role earn between $22.21 and $52.60 per hour, depending on experience, location, and employer.

What is a medical content reviewer?

A Medical Content Reviewer is responsible for evaluating medical and healthcare-related content to ensure accuracy, compliance, and clarity. They review scientific articles, marketing materials, or educational resources to verify that medical information is evidence-based and follows industry regulations. This role often requires expertise in medical writing, editing, and knowledge of healthcare guidelines. Medical Content Reviewers may work for pharmaceutical companies, healthcare organizations, or medical publishers. Their goal is to maintain the integrity and credibility of medical content for professional or public use.

What does a medical content reviewer do?

A typical day for a Medical Content Reviewer involves evaluating and editing clinical documents, educational materials, or pharmaceutical content for accuracy, clarity, and compliance with industry standards. You may collaborate with medical writers, subject matter experts, and regulatory teams to ensure materials are evidence-based and meet rigorous guidelines. Additional responsibilities often include fact-checking references, ensuring proper formatting, and providing feedback to authors. The work is both independent and team-oriented, and strong communication is crucial for maintaining consistency across projects and deadlines.

What are the key skills and qualifications needed to thrive as a medical content reviewer?

To thrive as a Medical Content Reviewer, you need a strong background in medical science or healthcare, experience with medical writing or editing, and thorough knowledge of clinical terminology and guidelines. Familiarity with reference management software, content management systems, and regulatory frameworks (such as ICMJE, AMA, or GPP guidelines) is often required, and certifications like a medical writing credential can be advantageous. Attention to detail, critical thinking, and strong communication skills make someone stand out in this position. These skills ensure the accuracy, clarity, and compliance of medical content, which is essential for informing healthcare professionals and patients alike.

What are popular job titles related to Medical Content Reviewer jobs in Raleigh, NC?

For Medical Content Reviewer jobs in Raleigh, NC, the most frequently searched job titles are:

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The top searched job categories for Medical Content Reviewer jobs in Raleigh, NC are:

Medical Content Reviewer jobs near you
Infographic showing various Medical Content Reviewer job openings in Raleigh, NC as of August 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 75% In-person, and 25% Remote job distribution, with an average salary of $85,034 per year, or $40.9 per hour.

Medical Writing Manager

micro1 AI

Raleigh, NC • Remote

$50 - $80/hr

Part-time

Posted 18 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