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Science Writer Jobs in Kentucky (NOW HIRING)

Medical Writing Manager

Lexington, KY Β· Remote

$50 - $80/hr

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

$90K - $130K/yr

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Technical Writer (Contractor) Contractor

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

$77K - $92K/yr

Job Title Medical Writer Department Study Set Up Location Remote East Coast | Must Sit in East Coast Hours Per Week 40 hours Schedule Days, Monday - Friday SUMMARY The Medical Writer is responsible

$55K - $126K/yr

Join a culture of empowerment and connectivity. Develop your craft Learn the skills you need to accelerate your career. Discover benefits that your life and work. Innovate with intention Build

New

Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow.

Posted Monday, August 31, 2026 at 4:00 AM ASRC Federal is a leading government contractor furthering missions in space, public health and defense. As an Alaska Native owned corporation, our work

$63K/yr

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Digital Writer Regular Full Time Atlanta,

Technical Writer (Mortgage / Fintech) Overview PhoenixTeam is seeking a Technical Writer with experience in mortgage and fintech platforms to create clear, accurate, and user-friendly documentation

Eagle Health Analytics (EHA) is seeking a Senior Technical Writer who will lead RFP (Request for Proposal), RFI/SSN (Request for Information/Sources Sought Notice), TOPR (Task Order Proposal Request)

$120K - $180K/yr

General Summary The Medical Writing Science Manager is responsible for preparing moderately complex clinical and regulatory documents and represents Medical Writing Science as a cross‑functional team

## Job Details: Senior Manager, Medical/Regulatory WriterFull details of the job.| | || --- | --- || | || | || --- | --- || | Senior Manager, Medical/Regulatory Writer || | VN831 || | Full Time || |

## Technical WriterApplylocations: USA - Ohio - Daytontime type: Full timeposted on: Posted Todayjob requisition id: REQ52294**Nordson Measurement & Control**, a global leader in Measurement &

Technical Writer shall: * Write, edit, and proofread technical documents, plans, reports, schedules, papers, and Microsoft Power Point presentations. The technical writer will conduct quality control

$66K - $86K/yr

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. TECHNICAL WRITER Hollywood, MD, US Salary

Description TheAmiveroTeam Amivero'steam of ITprofessionalsdelivers digital services that elevate the federal government, whether national security or improved government services. Our

Showing results 41-60

Science Writer information

See Kentucky salary details

$9.6K

$61.2K

$69K

How much do science writer jobs pay per year?

As of Sep 12, 2026, the average yearly pay for science writer in Kentucky is $61,231.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,200.00 and $64,300.00 per year, depending on experience, location, and employer.

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 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.

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.

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.

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 most commonly searched types of Science Writer jobs in Kentucky?

The most popular types of Science Writer jobs in Kentucky are:

What are popular job titles related to Science Writer jobs in Kentucky?

For Science Writer jobs in Kentucky, the most frequently searched job titles are:

What cities in Kentucky are hiring for Science Writer jobs?

Cities in Kentucky with the most Science Writer job openings:

What are popular job titles related to Science Writer jobs in KY?

For Science Writer jobs in KY, the most frequently searched job titles are:

Infographic showing various Science Writer job openings in Kentucky as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $61,231 per year, or $29.4 per hour.

Medical Writing Manager

Lexington, KY β€’ Remote

micro1 AI
Software DevelopmentΒ β€’Β 11 - 50 employees

$50 - $80/hr

Part-time

Re-posted 9 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 β€” 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 recordsβ€”tables, figures, listings, and protocolsβ€”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 β€” through your expert input, judgment, and real-world experience.