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Remote Biological Science Writer Jobs in Iowa (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 ...

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 ...

$75K - $89K/yr

Remote work within the United States may be considered only for employees not within commuting ... Bachelor's degree in policy, political science, biology or related field required. * A minimum of 5 ...

Remote micro1 is engaging Physics Experts (PhD / Postdoc) to contribute deep scientific knowledge ... Produce technically precise, clearly written solutions, detailing all assumptions, approximations ...

Remote micro1 is engaging Physics Experts (PhD / Postdoc) to contribute deep scientific knowledge ... Produce technically precise, clearly written solutions, detailing all assumptions, approximations ...

Showing results 41-60

Remote Biological Science Writer information

What does a remote biological science writer do?

A Remote Biological Science Writer creates scientific content related to biology, such as articles, reports, research summaries, or educational materials, while working from a location outside of a traditional office. They interpret complex biological research and translate it into clear, accessible language for various audiences, including scientists, healthcare professionals, and the general public. This role often involves collaborating with researchers, staying updated on scientific advancements, and ensuring accuracy and clarity in all written materials.

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

To thrive as a Remote Biological Science Writer, you need a solid background in biological sciences, excellent writing abilities, and typically at least a bachelor’s degree in a relevant field. Familiarity with scientific literature databases, reference management tools (like EndNote or Zotero), and proficiency in word processing and collaboration platforms are essential. Strong attention to detail, time management, and the ability to translate complex scientific concepts into clear, engaging language make someone stand out in this role. These skills ensure accurate, accessible content that meets publication standards and effectively communicates scientific information to varied audiences.

How does a remote biological science writer typically collaborate with researchers and editorial teams while working offsite?

As a Remote Biological Science Writer, you will frequently communicate with researchers, subject matter experts, and editorial teams through email, video conferencing, and project management tools. Regular virtual meetings help clarify project objectives, review scientific content, and ensure accuracy in interpretations. You may also participate in collaborative document editing and receive feedback through shared platforms to maintain alignment with publication standards. Building strong digital communication skills and being proactive in seeking input are essential for success in this remote, team-oriented environment.

What are popular job titles related to Remote Biological Science Writer jobs in Iowa?

For Remote Biological Science Writer jobs in Iowa, the most frequently searched job titles are:

What cities in Iowa are hiring for Remote Biological Science Writer jobs?

Cities in Iowa with the most Remote Biological Science Writer job openings:

Infographic showing various Remote Biological Science Writer job openings in Iowa as of August 2026, with employment types broken down into 6% Internship, 79% Full Time, 9% Part Time, and 6% Contract. Highlights an 100% Remote job distribution.

Medical Writing Manager

micro1 AI

Davenport, IA • Remote

$50 - $80/hr

Part-time

Posted 16 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.