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Scientific Medical Writer Jobs in Indiana (NOW HIRING)

micro1 AI

Medical Billing Specialist

Indianapolis, IN · 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 ...

micro1 AI

Medical Billing Specialist

South Bend, IN · 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 ...

Indiana University

Technical Writer

Bloomington, IN · On-site

... scientific and medical knowledge. * Provides expertise on regulatory requirements and ensures ... Technical Writing Click here to learn more about Indiana University's Job Framework. Posting ...

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Scientific Medical Writer information

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How much do scientific medical writer jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for scientific medical writer in Indiana is $44.03, according to ZipRecruiter salary data. Most workers in this role earn between $32.02 and $53.32 per hour, depending on experience, location, and employer.

What is a scientific medical writer?

A Scientific Medical Writer creates clear, accurate, and well-structured documents related to medical and scientific information. They translate complex research data into formats such as journal articles, regulatory documents, clinical study reports, and educational materials. These professionals work closely with researchers, healthcare professionals, and regulatory teams to ensure scientific accuracy and compliance with industry guidelines. Strong writing skills, scientific knowledge, and attention to detail are essential for success in this role.

What are the typical work settings and team dynamics for a scientific medical writer?

Scientific Medical Writers commonly work in pharmaceutical companies, medical communications agencies, academic institutions, or as independent consultants, often collaborating within cross-functional teams that include researchers, clinicians, regulatory experts, and marketing professionals. Daily responsibilities involve drafting, reviewing, and revising scientific manuscripts, clinical study reports, and regulatory documents, often under tight deadlines. While some positions are office-based, there are increasing opportunities for remote or hybrid work environments. Collaboration, adaptability, and regular communication with subject matter experts are central to success in this field, as writers must ensure both scientific accuracy and audience-appropriate messaging.

What are the key skills and qualifications needed to thrive in a scientific medical writer position, and why are they important?

To thrive as a Scientific Medical Writer, you need advanced scientific knowledge, exceptional writing and editing abilities, and typically a degree in life sciences or a related field. Familiarity with reference management software, publication guidelines (such as GPP or ICMJE), and medical literature databases is highly beneficial. Attention to detail, strong project management, and clear communication skills help differentiate top performers in this role. These competencies ensure the accurate, compliant, and effective communication of complex scientific information to a variety of audiences.

How to become a scientific medical writer?

To become a scientific medical writer, typically a bachelor's degree in a life science or related field is required, often complemented by advanced degrees such as a master's or PhD. Developing strong writing skills, understanding scientific research, and gaining experience through internships or entry-level positions are important steps; familiarity with medical terminology and tools like reference management software can also be beneficial.

Is there a demand for scientific medical writers?

There is strong demand for scientific medical writers due to the growth of the healthcare and pharmaceutical industries, as well as increased regulatory requirements for clinical documentation and medical communications. Professionals with expertise in scientific writing, knowledge of medical terminology, and familiarity with industry tools are sought after in both pharmaceutical companies and contract research organizations.

What are popular job titles related to Scientific Medical Writer jobs in Indiana?

For Scientific Medical Writer jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Scientific Medical Writer jobs in Indiana look for?

The top searched job categories for Scientific Medical Writer jobs in Indiana are:

What cities in Indiana are hiring for Scientific Medical Writer jobs?

Cities in Indiana with the most Scientific Medical Writer job openings:

Scientific Medical Writer jobs near you
Infographic showing various Scientific Medical Writer job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, and 6% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $91,574 per year, or $44 per hour.

Medical Billing Specialist

micro1 AI

Indianapolis, IN • Remote

$50 - $80/hr

Part-time

Posted 19 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