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Medical Science Writer Jobs in Tennessee (NOW HIRING)

micro1 AI

Medical Writing Manager

Knoxville, TN · Remote

$50 - $80/hr

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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Medical Science Writer information

How does a medical science writer typically collaborate with subject matter experts and project teams?

Medical Science Writers frequently work with physicians, researchers, and regulatory professionals to create accurate and clear scientific documents. Collaboration often involves conducting interviews, reviewing complex data, and ensuring all materials meet industry and regulatory standards. Writers may participate in team meetings, provide content drafts for review, and incorporate feedback from multiple stakeholders. This collaborative environment helps ensure the final documents are scientifically rigorous and tailored to the intended audience, whether that be regulatory agencies, healthcare professionals, or the public.

Is there a demand for medical science writers?

Medical science writers are in high demand due to the growing need for clear communication of complex scientific and medical information. They are employed in pharmaceutical companies, healthcare organizations, and research institutions, often requiring strong writing skills and knowledge of scientific tools and regulations. The field is expected to grow as medical research and healthcare industries expand globally.

Do medical science writers make good money?

Medical science writers typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions may start around $60,000 annually, while experienced writers with specialized knowledge can earn over $100,000. The role often requires strong writing skills, scientific knowledge, and familiarity with industry tools like reference management software.

What are the key skills and qualifications needed to thrive as a medical science writer, and why are they important?

To thrive as a Medical Science Writer, you need a solid background in life sciences or medicine (often with an advanced degree), strong writing skills, and the ability to interpret complex scientific data. Familiarity with referencing software, medical databases, and style guides such as AMA or ICMJE is typically required. Attention to detail, critical thinking, and the ability to communicate clearly with both scientific and non-scientific audiences are essential soft skills. These competencies ensure accurate, credible, and accessible medical content that supports both regulatory compliance and effective information dissemination.

How to become a medical science writer?

To become a medical science writer, typically a bachelor's degree in life sciences, health sciences, or a related field is required, often complemented by strong writing skills and knowledge of scientific concepts. Gaining experience through internships, developing expertise in medical terminology, and familiarizing oneself with scientific publishing tools can enhance prospects. Advanced degrees or certifications in science communication can also be beneficial.

What is a medical science writer?

Medical Science Writers are professionals who create scientific documents related to medicine, healthcare, and clinical research. They translate complex scientific and clinical information into clear, accurate, and accessible content for various audiences, such as healthcare professionals, regulatory agencies, or the general public. Their work includes writing research articles, regulatory documents, educational materials, and marketing content. Medical Science Writers often work for pharmaceutical companies, medical communication agencies, academic institutions, or as freelancers.
What are popular job titles related to Medical Science Writer jobs in Tennessee? For Medical Science Writer jobs in Tennessee, the most frequently searched job titles are:
What job categories do people searching Medical Science Writer jobs in Tennessee look for? The top searched job categories for Medical Science Writer jobs in Tennessee are:
Medical Science Writer jobs near you
Infographic showing various Medical Science Writer job openings in Tennessee as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution.

Medical Writing Manager

micro1 AI

Knoxville, TN • Remote

$50 - $80/hr

Part-time

Posted 5 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