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Medical Writer Oncology Jobs (NOW HIRING)

QC Medical Writer

$100K - $126K/yr

This position reports to Executive Director, Medical Writing Oncology and is part of the Medical Writing Function. We are currently seeking a dynamic, highly motivated, and experienced individual for ...

QC Medical Writer

$100K - $126K/yr

This position reports to Executive Director, Medical Writing Oncology and is part of the Medical Writing Function. We are currently seeking a dynamic, highly motivated, and experienced individual for ...

Medical Writer - Remote

Austin, TX ยท Remote

$50 - $90/hr

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Experience in oncology and haematology is preferred.

Medical Writer - Remote

New York, NY ยท Remote

$50 - $80/hr

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Experience in oncology and haematology is preferred.

Medical Writer - Remote

Atlanta, GA ยท Remote

$50 - $90/hr

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Experience in oncology and haematology is preferred.

Medical Writer - Remote

Seattle, WA ยท Remote

$50 - $90/hr

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Experience in oncology and haematology is preferred.

Medical Writer - Remote

Seattle, WA ยท Remote

$50 - $90/hr

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Experience in oncology and haematology is preferred.

Medical Writer - Remote

Chicago, IL ยท Remote

$50 - $90/hr

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Experience in oncology and haematology is preferred.

Medical Writer - Remote

Boston, MA ยท Remote

$50 - $90/hr

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Experience in oncology and haematology is preferred.

Medical Writer - Remote

Phoenix, AZ ยท Remote

$50 - $90/hr

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Experience in oncology and haematology is preferred.

Medical Writer - Remote

Houston, TX ยท Remote

$50 - $90/hr

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Experience in oncology and haematology is preferred.

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Medical Writer Oncology information

See salary details

$11

$46

$78

How much do medical writer oncology jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for 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 is a medical writer oncology?

A Medical Writer in Oncology is responsible for creating, editing, and reviewing scientific documents related to cancer research, treatments, and clinical trials. They work with researchers, physicians, and pharmaceutical companies to develop regulatory submissions, manuscripts, medical education materials, and more. This role requires a strong understanding of oncology, medical terminology, and scientific writing standards. Medical Writers ensure complex medical information is communicated clearly and accurately for various audiences, including healthcare professionals, regulatory agencies, and patients.

What does a medical writer oncology do?

Medical Writers specializing in oncology often spend their days researching scientific literature, drafting and editing clinical documents such as protocols, clinical study reports, and regulatory submissions, and ensuring accuracy and compliance with industry standards. They frequently collaborate with clinical researchers, medical experts, and regulatory teams to clarify scientific data and meet project deadlines. Depending on the organization, you may also participate in team meetings to discuss project progress, address feedback from stakeholders, and support scientific publications or presentations. This dynamic role requires balancing multiple projects and adapting quickly to new data or shifting priorities.

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

To thrive as a Medical Writer Oncology, you need an advanced understanding of oncology, scientific research, and medical terminology, typically supported by a life sciences degree or higher and strong writing skills. Familiarity with referencing software, publication management systems, and guidelines such as ICMJE or GPP is important, and some roles may require certification from the American Medical Writers Association (AMWA) or similar organizations. Excellent communication, attention to detail, and the ability to interpret complex data are crucial soft skills in this field. These abilities are vital for producing accurate, clear, and regulatory-compliant documents that support scientific communication and drug development in oncology.

What cities are hiring for Medical Writer Oncology jobs?

Cities with the most Medical Writer Oncology job openings:

What are the most commonly searched types of Medical Writer Oncology jobs?

The most popular types of Medical Writer Oncology jobs are:

What states have the most Medical Writer Oncology jobs?

States with the most job openings for Medical Writer Oncology jobs include:

Infographic showing various Medical Writer Oncology job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 83% In-person, and 17% Remote job distribution, with an average salary of $96,235 per year, or $46.3 per hour.

[Voronoi, Inc.] Medical Writer (Hybrid Work)

VORONOI, Inc.

Cambridge, MA โ€ข On-site

$110 - $170/hr

Other

Posted yesterday

New


Job description

[Voronoi, Inc.] Medical Writer (Hybrid Work)

Medical Writer - Oncology Clinical Trials

Location: minimum 2 days onsite in Waltham, MA office Cambridge / Greater Boston

Position Summary:

We are seeking an experienced Medical Writer with a strong background in oncology clinical trials to join our growing company. The ideal candidate will have a deep understanding of oncology therapeutic areas and a proven track record of preparing high-quality regulatory and scientific documents in support of clinical development programs.

Key Responsibilities:
  • Develop, write, and edit clinical and regulatory documents related to oncology clinical trials, including but not limited to:
  • Clinical study protocols and amendments
  • Investigator brochures
  • Clinical study reports (CSRs)
  • Informed consent forms
  • Briefing documents
  • Clinical sections of INDs, NDAs, BLAs, and other regulatory submissions
  • Collaborate with cross-functional teams including Clinical Development, Regulatory Affairs, Biostatistics, Data Management, and Safety teams to ensure content accuracy and consistency
  • Interpret and synthesize complex clinical and scientific data into clear, concise, and scientifically sound documents
  • Ensure all documents comply with ICH guidelines, regulatory requirements, and internal SOPs
  • Participate in strategic planning and document timelines
  • Mentor junior medical writers or contractors as needed
  • Stay current with therapeutic area developments, industry trends, and regulatory guidance
Qualifications:
  • Advanced degree (PhD, PharmD, MD, or MSc) in life sciences, medicine, or a related field
  • Minimum 5 years of medical writing experience, with at least 3 years focused on oncology clinical trials
  • In-depth understanding of oncology disease areas and clinical endpoints
  • Extensive experience in authoring documents for Phase Iโ€“III oncology trials and regulatory submissions
  • Strong knowledge of ICH-GCP, FDA/EMA guidelines, and clinical trial processes
  • Excellent written and verbal communication skills
  • High attention to detail, strong analytical skills, and ability to manage multiple projects under tight deadlines
  • Proficiency with document management systems and MS Office Suite; experience with templates and style guides
Preferred Qualifications:
  • Experience working in a CRO, biotech, or pharmaceutical company
  • Familiarity with submission processes (eCTD) and regulatory publishing
  • Membership in professional organizations such as AMWA or EMWA is preferred
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