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$78

How much do part time medical writer oncology jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for part time medical writer oncology in the United States is $46.27, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $56.01 per hour, depending on experience, location, and employer.

What does a part time medical writer in oncology do?

A Part Time Medical Writer in Oncology is responsible for creating scientific documents, such as research articles, clinical study reports, regulatory submissions, and educational materials focused on cancer research and treatment. They work with subject matter experts, interpret complex data, and translate it into clear, accurate content tailored for healthcare professionals or regulatory agencies. This role often requires strong writing skills, attention to detail, and a good understanding of oncology terminology and current research trends.

What are the key skills and qualifications needed to thrive as a part time medical writer in oncology?

To thrive as a Part Time Medical Writer in Oncology, you need a solid background in life sciences or medicine, with expertise in oncology and strong written communication skills, often supported by an advanced degree or relevant certification. Familiarity with referencing software, scientific databases, and guidelines like ICMJE or GPP are typically required. Attention to detail, time management, and the ability to translate complex scientific data into clear, accurate content are standout soft skills in this role. These competencies ensure the production of high-quality, compliant documents that effectively communicate critical oncology information to diverse audiences.

What are some of the common challenges faced by part time medical writers specializing in oncology, and how can they effectively manage them?

Part-time medical writers in oncology often navigate the challenge of staying current with rapidly evolving research while balancing limited work hours. Managing tight deadlines, complex scientific data, and frequent collaboration with oncologists and researchers can also be demanding. To succeed, it's helpful to develop strong organizational skills, set clear communication channels with team members, and prioritize ongoing learning in oncology trends. Leveraging digital collaboration tools and attending relevant webinars or conferences can further enhance efficiency and knowledge in this specialized field.

What is the difference between Part Time Medical Writer Oncology vs Part Time Medical Writer Hematology?

AspectPart Time Medical Writer OncologyPart Time Medical Writer Hematology
Required CredentialsMedical or life sciences degree, writing experience in oncologyMedical or life sciences degree, writing experience in hematology
Work EnvironmentPharmaceutical companies, CROs, medical communicationsPharmaceutical companies, CROs, medical communications
Industry UsageFocus on cancer treatments, clinical trial documentationFocus on blood disorders, clinical trial documentation
Search & Comparison IntentPart Time Medical Writer Oncology vs Part Time Medical Writer Hematology

Both roles involve medical writing in the pharmaceutical industry, requiring similar credentials and work environments. The key difference lies in their specialization: Oncology focuses on cancer-related therapies, while Hematology centers on blood disorders. Candidates should choose based on their expertise and interest in the specific medical field.

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Cities with the most Part Time Medical Writer Oncology job openings:

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Part Time Medical Writer Oncology jobs near you
Infographic showing various Part Time Medical Writer Oncology job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $96,235 per year, or $46.3 per hour.

Medical Writer / Clinical Document Author

micro1 AI

Billings, MT • Remote

$50 - $80/hr

Part-time

Posted 14 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