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Clinical Content Manager Jobs in Nebraska (NOW HIRING)

Air Methods

NE · On-site

$81K - $122K/yr

Develop and assist with scenario and clinical content for new hires and recurrent clinical ... Support the implementation of management decisions that affect air medical practice in the clinical ...

Air Methods

NE · On-site

$81K - $122K/yr

Develop and assist with scenario and clinical content for new hires and recurrent clinical ... Support the implementation of management decisions that affect air medical practice in the clinical ...

micro1 AI

Medical Writing Manager

Lincoln, NE · Remote

$50 - $80/hr

Apply expert judgment to assess whether AI-generated content fulfills clinical template and ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

micro1 AI

Medical Writing Manager

Omaha, NE · Remote

$50 - $80/hr

Apply expert judgment to assess whether AI-generated content fulfills clinical template and ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

micro1 AI

Medical Billing Specialist

Lincoln, NE · Remote

$50 - $80/hr

... content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management. * Evaluate scientific accuracy in ...

micro1 AI

Medical Billing Specialist

Omaha, NE · Remote

$50 - $80/hr

... content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management. * Evaluate scientific accuracy in ...

Bryan Health

Coding Specialist III

Kearney, NE · On-site

Possesses the knowledge and skills to thoroughly review the clinical content of all levels of ... Management Association (AHIMA) and adheres to all Official Coding Guidelines. 15. Maintains ...

Bryan Health

Coding Specialist III

Kearney, NE · On-site

Possesses the knowledge and skills to thoroughly review the clinical content of all levels of ... Management Association (AHIMA) and adheres to all Official Coding Guidelines. 15. Maintains ...

Faith Health

RN Clinical Educator

Norfolk, NE · On-site

... objectives, content outline, teaching method and evaluation. 2. Selects content, faculty, and ... management system. 11. Understands and assists with operation of audiovisual equipment within ...

Bryan Health

Coding Specialist III

Lincoln, NE

Possesses the knowledge and skills to thoroughly review the clinical content of all levels of ... Management Association (AHIMA) and adheres to all Official Coding Guidelines. 15. Maintains ...

Bryan Health

Coding Specialist III

Lincoln, NE · On-site

Possesses the knowledge and skills to thoroughly review the clinical content of all levels of ... Management Association (AHIMA) and adheres to all Official Coding Guidelines. 15. Maintains ...

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All JobsClinical Content JobsClinical Content Manager JobsClinical Content Manager Jobs in Nebraska

Clinical Content Manager information

What is a clinical content manager?

A Clinical Content Manager is a healthcare professional responsible for developing, reviewing, and managing clinical content for medical platforms, electronic health records, or healthcare publications. They ensure that clinical information is accurate, up-to-date, and aligns with current medical guidelines and regulations. Clinical Content Managers often collaborate with clinicians, editors, and IT teams to improve the quality and accessibility of healthcare information. Their work is vital in supporting clinical decision-making and enhancing patient care.

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

To thrive as a Clinical Content Manager, you need a solid background in healthcare or life sciences, strong writing and editing abilities, and experience in clinical or medical content development. Familiarity with content management systems (CMS), medical databases, and regulatory guidelines such as HIPAA or FDA requirements is typically required. Outstanding attention to detail, project management skills, and the ability to communicate complex information clearly set top candidates apart. These competencies ensure the creation of accurate, compliant, and engaging clinical content that supports organizational goals and regulatory standards.

How does a clinical content manager typically collaborate with medical professionals and cross-functional teams?

Clinical Content Managers frequently work closely with physicians, subject matter experts, and regulatory teams to ensure that all content is clinically accurate, compliant, and tailored for the intended audience. They participate in regular meetings to gather expert input and feedback, coordinate with editors and designers for content delivery, and often serve as a bridge between clinical teams and non-clinical stakeholders. This collaborative environment ensures content aligns with the latest clinical guidelines and organizational goals, while also fostering professional growth through exposure to diverse healthcare perspectives.

What are popular job titles related to Clinical Content Manager jobs in Nebraska?

For Clinical Content Manager jobs in Nebraska, the most frequently searched job titles are:

What job categories do people searching Clinical Content Manager jobs in Nebraska look for?

The top searched job categories for Clinical Content Manager jobs in Nebraska are:

What cities in Nebraska are hiring for Clinical Content Manager jobs?

Cities in Nebraska with the most Clinical Content Manager job openings:

Clinical Content Manager jobs near you
Infographic showing various Clinical Content Manager job openings in Nebraska as of August 2026, with employment types broken down into 83% Full Time, 16% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution.

Medical Writer / Clinical Document Author

micro1 AI

Omaha, NE • Remote

$50 - $80/hr

Part-time

Re-posted 4 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