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Clinical Content Writer Jobs in Indiana (NOW HIRING)

micro1 AI

Medical Writing Manager

Evansville, IN · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Apply expert judgment to assess whether AI-generated content fulfills clinical template and ...

micro1 AI

Medical Writing Manager

Carmel, IN · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Apply expert judgment to assess whether AI-generated content fulfills clinical template and ...

micro1 AI

Medical Writing Manager

Fishers, IN · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Apply expert judgment to assess whether AI-generated content fulfills clinical template and ...

micro1 AI

Medical Writing Manager

Fort Wayne, IN · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Apply expert judgment to assess whether AI-generated content fulfills clinical template and ...

micro1 AI

Medical Writing Manager

Indianapolis, IN · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Apply expert judgment to assess whether AI-generated content fulfills clinical template and ...

micro1 AI

Medical Writing Manager

South Bend, IN · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Apply expert judgment to assess whether AI-generated content fulfills clinical template and ...

Hearst

Clinical Pharmacist

Carmel, IN · On-site

$112K - $134K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

In This One, You Write History. Join the healthcare information technology team that's turning drug ... Responsible for maintaining assigned clinical content using established procedures, clinical ...

Hearst Communications, Inc.

Clinical Pharmacist

Carmel, IN · On-site

$112K - $134K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

In This One, You Write History. Join the healthcare information technology team that's turning drug ... Responsible for maintaining assigned clinical content using established procedures, clinical ...

Hearst Newspapers

Clinical Pharmacist

Indianapolis, IN · On-site

$113K - $135K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

In This One, You Write History. Join the healthcare information technology team that's turning drug ... Responsible for maintaining assigned clinical content using established procedures, clinical ...

First Databank

Clinical Pharmacist

Carmel, IN · On-site

$112K - $134K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

In This One, You Write History. Join the healthcare information technology team that's turning drug ... Responsible for maintaining assigned clinical content using established procedures, clinical ...

Hearst

Clinical Pharmacist

Carmel, IN · On-site

$112K - $134K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

In This One, You Write History. Join the healthcare information technology team that's turning drug ... Responsible for maintaining assigned clinical content using established procedures, clinical ...

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All JobsClinical Content Writer JobsClinical Content Writer Jobs in Indiana

Clinical Content Writer information

What is a clinical content writer?

A Clinical Content Writer is a professional who creates, edits, and reviews medical and healthcare-related content for various audiences. They often have a background in healthcare, medicine, or life sciences, and use their expertise to ensure that content is accurate, clear, and compliant with relevant regulations. Their work includes writing patient education materials, clinical guidelines, medical articles, and marketing content for healthcare organizations. Clinical Content Writers play a key role in bridging the gap between complex medical information and the needs of patients, healthcare professionals, and the general public.

What is the difference between Clinical Content Writer vs Medical Writer?

AspectClinical Content WriterMedical Writer
CredentialsOften requires a background in healthcare, life sciences, or related fields; certifications like ACRP or RAC can be beneficialTypically holds degrees in life sciences, medicine, or related fields; certifications like AMWA or DIA are common
Work EnvironmentWorks in healthcare, pharmaceutical, or biotech companies, focusing on clinical trial documentation and regulatory submissionsWorks in pharmaceutical, biotech, or medical communication agencies, creating a variety of medical and scientific content
Employer & Industry UsageUsed mainly in clinical research, regulatory affairs, and healthcare settingsUsed across medical communications, regulatory, and scientific publishing sectors

In summary, Clinical Content Writers focus on creating clinical trial documents and regulatory content within healthcare and research settings, while Medical Writers produce a broader range of scientific and medical content across various industries. Both roles require strong scientific knowledge and writing skills but differ in their specific focus and work environment.

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

To thrive as a Clinical Content Writer, you need strong medical writing skills, a background in healthcare or life sciences, and familiarity with evidence-based research. Proficiency in tools like Microsoft Office, referencing software (e.g., EndNote), and content management systems is often required, along with knowledge of industry guidelines. Excellent attention to detail, strong organizational abilities, and the capacity to communicate complex concepts clearly are essential soft skills. These competencies ensure high-quality, accurate, and accessible clinical content that supports healthcare professionals and patient education.

How does a clinical content writer typically collaborate with healthcare professionals and subject matter experts?

Clinical Content Writers frequently work alongside physicians, nurses, and other healthcare specialists to ensure that written materials are accurate, evidence-based, and appropriate for the target audience. Collaboration usually involves interviews, document reviews, and feedback sessions to clarify complex medical concepts and maintain compliance with regulatory standards. Building strong professional relationships and maintaining open communication are essential for producing clear and reliable clinical content.

What are popular job titles related to Clinical Content Writer jobs in Indiana?

For Clinical Content Writer jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Clinical Content Writer jobs in Indiana look for?

The top searched job categories for Clinical Content Writer jobs in Indiana are:

What cities in Indiana are hiring for Clinical Content Writer jobs?

Cities in Indiana with the most Clinical Content Writer job openings:

Clinical Content Writer jobs near you

Medical Writer / Clinical Document Author

micro1 AI

Indianapolis, IN • Remote

$50 - $80/hr

Part-time

Posted 12 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