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Clinical Writer Jobs in Georgia (NOW HIRING)

YO AI Labs

Clinical Document Author - Remote

Atlanta, GA · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview We are seeking an experienced Medical Writer / Clinical Document Author to develop ...

YO AI Labs

Medical Writer - Remote

Atlanta, GA · Remote

$50 - $90/hr

Contractor Pay: $50-$80/hour Job Overview We are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring ...

Artivion

Senior Medical Writer

Kennesaw, GA · On-site

Writing clinical regulatory documents including annual reports, study summaries, and other study rationales. * Support clinical requirements for regulatory submissions and maintenance. * Coordinating ...

CryoLife

Senior Medical Writer

Kennesaw, GA · On-site

Writing clinical regulatory documents including annual reports, study summaries, and other study rationales. * Support clinical requirements for regulatory submissions and maintenance. * Coordinating ...

MMS

Senior Medical Writer (Remote)

Atlanta, GA · On-site

Write and edit clinical development documents, including but not limited to, clinical protocols, investigator's brochures, clinical study reports, subject consent forms, integrated safety and ...

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Clinical Writer information

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How much do clinical writer jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for clinical writer in Georgia is $45.89, according to ZipRecruiter salary data. Most workers in this role earn between $33.70 and $54.18 per hour, depending on experience, location, and employer.

What is a clinical writer?

A Clinical Writer is a professional who creates, edits, and manages medical and scientific documents related to clinical research, healthcare, and pharmaceuticals. They often prepare clinical study reports, regulatory submissions, patient information leaflets, and scientific manuscripts. Clinical Writers work closely with researchers, physicians, and regulatory professionals to ensure that complex clinical information is communicated clearly, accurately, and in compliance with industry standards. Their work is essential for documenting clinical trials and supporting the approval of new drugs or therapies.

What are the key skills and qualifications needed to thrive as a clinical writer?

To thrive as a Clinical Writer, you need a solid background in life sciences or medical fields, excellent writing skills, and attention to detail, often supported by a relevant degree. Familiarity with regulatory guidelines, literature databases, and tools like EndNote, as well as certifications such as AMWA or EMWA, are highly valued. Strong communication, critical thinking, and time management help Clinical Writers convey complex information clearly and collaborate with medical professionals. These skills ensure the accuracy, clarity, and compliance of clinical documents critical for regulatory submissions and advancing medical knowledge.

What are some common challenges clinical writers face when translating complex medical research into accessible documents?

Clinical writers often encounter the challenge of interpreting highly technical and data-rich research while ensuring accuracy and regulatory compliance. Balancing the need for scientific precision with the ability to communicate information clearly to various audiences—such as healthcare professionals, regulatory agencies, or patients—requires strong analytical and communication skills. Additionally, clinical writers must stay updated on evolving guidelines and collaborate closely with subject matter experts, which can be demanding but also enriches their expertise and professional network.

Do clinical writers make good money?

Clinical writers typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions may start around $60,000 annually, while experienced professionals can earn over $100,000, especially with specialized knowledge in regulatory writing or medical sciences.

How can I get into clinical writing with no experience?

Clinical writers create scientific documents for healthcare and pharmaceutical industries. To enter the field with no experience, gaining knowledge of medical terminology, regulatory guidelines, and writing skills through online courses or certifications can be helpful. Building a portfolio with sample documents and seeking entry-level or freelance opportunities can also improve chances of breaking into clinical writing.

What are popular job titles related to Clinical Writer jobs in Georgia?

For Clinical Writer jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Clinical Writer jobs in Georgia look for?

The top searched job categories for Clinical Writer jobs in Georgia are:

What cities in Georgia are hiring for Clinical Writer jobs?

Cities in Georgia with the most Clinical Writer job openings:

What are popular job titles related to Clinical Writer jobs in GA?

For Clinical Writer jobs in GA, the most frequently searched job titles are:

Clinical Writer jobs near you
Infographic showing various Clinical Writer job openings in Georgia as of August 2026, with employment types broken down into 56% Full Time, and 44% Part Time. Highlights an 89% In-person, and 11% Remote job distribution, with an average salary of $95,455 per year, or $45.9 per hour.

Clinical Document Author - Remote

YO AI Labs

Atlanta, GA • Remote

$50 - $80/hr

Full-time

Posted 5 days ago

Job description

Job Title: Medical Writer / Clinical Document Author

Location: Remote
Job Type: Contractor
Pay: $50–$80/hour

Job Overview

We are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing.

Key Responsibilities

  • Author and review Clinical Study Reports (CSRs) and other regulatory documents.

  • Interpret clinical protocols and ensure compliance with ICH guidelines.

  • Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.

  • Review safety documentation, including DSURs and PSURs/PBRERs.

  • Provide structured feedback and collaborate with cross-functional teams.

  • Support AI-assisted documentation evaluation and quality improvement initiatives.

Required Skills

  • Regulatory Medical Writing

  • Clinical Study Report (CSR) Authoring

  • ICH E3 Guidelines

  • Scientific Accuracy Assessment

  • Source Data Verification

  • Clinical Protocol Interpretation

  • TFL Analysis

  • eCTD Knowledge

  • Strong Written Communication & Collaboration

Qualifications

  • 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment.

  • Experience authoring Clinical Study Reports and regulatory documentation.

  • Strong knowledge of ICH E3, ICH E2F, ICH E2C, and eCTD requirements.

  • Advanced degree in Life Sciences, Pharmacy, Medicine, or a related field (MD, PharmD, PhD, or MSc).

  • Experience in oncology and haematology is preferred.