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Science Writer Jobs in Columbus, GA (NOW HIRING)

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

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Field Scientist

Columbus, GA · On-site

$65K - $86K/yr

Drafts written proposals to clients for small projects and may assist with portions of proposals on ... Bachelor's degree in Environmental Science or related science field and a minimum 1 year related ...

Field Scientist

Columbus, GA

$67K - $88K/yr

Bachelor's degree in Environmental Science or related science field and a minimum 1 year related ... Drafts written proposals to clients for small projects and may assist with portions of proposals on ...

Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content. * Advanced degree in life sciences, pharmacy, or medicine (PhD ...

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Science Writer information

See Columbus, GA salary details

$9.8K

$63.1K

$71.2K

How much do science writer jobs pay per year?

As of Aug 7, 2026, the average yearly pay for science writer in Columbus, GA is $63,106.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,000.00 and $66,200.00 per year, depending on experience, location, and employer.

How much do science writers get paid?

Science writers' salaries vary based on experience, education, and location, but typically range from $45,000 to $85,000 annually. Freelance science writers may earn per project or word, with rates often between $0.10 and $1.00 per word. Experienced writers with specialized knowledge or advanced degrees can earn higher salaries or project fees.

How to become a science writer?

To become a science writer, individuals typically need a strong background in science, often a bachelor's degree in a related field, along with excellent writing skills. Gaining experience through internships, freelance writing, or contributing to science publications can help build a portfolio. Familiarity with scientific concepts, research methods, and tools like data visualization or editing software is also beneficial.

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

To thrive as a Science Writer, you need a solid background in scientific concepts, strong research abilities, and exceptional writing and editing skills, often supported by a degree in science or journalism. Familiarity with citation management tools, content management systems, and scientific databases is usually required. Attention to detail, creativity, and the ability to communicate complex ideas clearly are essential soft skills that set outstanding candidates apart. These competencies are crucial for crafting accurate, engaging, and accessible content that effectively bridges the gap between scientific experts and the general public.

Are science writers in demand?

Science writers are in steady demand as organizations seek clear communication of complex scientific information for audiences such as the public, policymakers, and industry professionals. Employment opportunities are often available in media outlets, research institutions, and science-focused organizations, with success often relying on strong writing skills and familiarity with scientific topics.

What are some typical challenges science writers face in this role?

Science Writers often encounter the challenge of translating complex scientific concepts into clear, compelling language for a broader audience without compromising accuracy. They must stay up-to-date with the latest research and frequently juggle tight deadlines while coordinating with subject matter experts and editors. Additionally, working in a fast-paced environment sometimes requires quick adaptation to new topics or publication formats. Overcoming these challenges sharpens communication skills, broadens subject expertise, and builds a portfolio of diverse, high-impact work.

What is a science writer?

A Science Writer researches, writes, and edits content about scientific topics for various audiences. They translate complex scientific information into clear and engaging articles, reports, or scripts for publications, websites, and media outlets. Science Writers may work for universities, research organizations, media companies, or as freelancers. Their work helps bridge the gap between scientists and the public by making scientific discoveries and advancements accessible and understandable.

What are popular job titles related to Science Writer jobs in Columbus, GA? For Science Writer jobs in Columbus, GA, the most frequently searched job titles are:
What job categories do people searching Science Writer jobs in Columbus, GA look for? The top searched job categories for Science Writer jobs in Columbus, GA are:
What cities near Columbus, GA are hiring for Science Writer jobs? Cities near Columbus, GA with the most Science Writer job openings:
Infographic showing various Science Writer job openings in Columbus, GA as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 67% Full Time, 29% Part Time, and 2% Contract. Highlights an 77% Physical, 3% Hybrid, and 20% Remote job distribution, with an average salary of $63,106 per year, or $30.3 per hour.

Medical Writer / Clinical Document Author

micro1 AI

Columbus, GA • Remote

$50 - $80/hr

Part-time

Posted 3 days ago

New


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.