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Oncology Content Writer Jobs (NOW HIRING)

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Oncology Content Writer information

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How much do oncology content writer jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for oncology content writer in the United States is $40.46, according to ZipRecruiter salary data. Most workers in this role earn between $23.56 and $46.39 per hour, depending on experience, location, and employer.

What does an oncology content writer do?

An Oncology Content Writer specializes in creating educational and informative materials about cancer, treatments, research advances, and patient care. They develop content for websites, brochures, articles, newsletters, and other resources to help patients, healthcare professionals, and the public understand complex oncology topics. Their work often involves collaborating with medical experts to ensure accuracy and using plain language to make information accessible. This role requires a strong background in writing, research, and often some knowledge of medical or scientific terminology.

What are the key skills and qualifications needed to thrive as an oncology content writer?

To thrive as an Oncology Content Writer, you need a solid background in medical writing, oncology knowledge, and a relevant degree in life sciences, communications, or journalism. Familiarity with referencing tools, style guides (such as AMA or AP), and content management systems is typically required. Exceptional research, attention to detail, and the ability to communicate complex information clearly are valuable soft skills. These skills ensure the delivery of accurate, accessible, and trustworthy oncology content for both medical professionals and patients.

How does an oncology content writer typically collaborate with medical professionals and subject matter experts?

As an Oncology Content Writer, you will frequently partner with oncologists, researchers, and other healthcare professionals to ensure the accuracy and clarity of your content. This often involves conducting interviews, reviewing medical literature, and seeking feedback on drafts to translate complex oncology topics into accessible, patient-friendly materials. Strong communication and relationship-building skills are essential, as is the ability to synthesize technical information while adhering to editorial and regulatory guidelines. Collaboration is key to producing trustworthy and impactful content that meets both clinical standards and audience needs.

What are popular job titles related to Oncology Content Writer jobs?

For Oncology Content Writer jobs, the most frequently searched job titles are:

Infographic showing various Oncology Content Writer job openings in the United States as of September 2026, with employment types broken down into 2% Internship, 71% Full Time, 24% Part Time, 1% Temporary, and 2% Contract. Highlights an 71% Physical, 3% Hybrid, and 26% Remote job distribution, with an average salary of $84,151 per year, or $40.5 per hour.

Medical Writer / Clinical Document Author

Huntsville, AL โ€ข Remote

micro1 AI
Software Developmentย โ€ขย 11 - 50 employees

$50 - $80/hr

Part-time

Re-posted 6 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 customerโ€™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 โ€” 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 recordsโ€”tables, figures, listings, and protocolsโ€”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 โ€” through your expert input, judgment, and real-world experience.