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Remote Oncology Medical Writer Jobs (NOW HIRING)

Veristat

... oncology projects in the past 5 years 350+ rare disease projects delivered in the past 5 years ... Benefits vary by location and may include: o Remote working o Flexible time off o Paid holidays o ...

Veristat

Principal Medical Writer

Scotland, PA · On-site +1

... oncology projects in the past 5 years 350+ rare disease projects delivered in the past 5 years ... Benefits vary by location and may include: o Remote working o Flexible time off o Paid holidays o ...

Veristat

Principal Medical Writer

Columbia, SC · On-site +1

... oncology projects in the past 5 years 350+ rare disease projects delivered in the past 5 years ... Benefits vary by location and may include: o Remote working o Flexible time off o Paid holidays o ...

Sumitomo Pharma

QC Medical Writer

$100K - $126K/yr

This position reports to Executive Director, Medical Writing Oncology and is part of the Medical ... Primarily remote role with periodic on-site meetings in office. Must be able to travel domestically ...

Sumitomopharma

QC Medical Writer

$100K - $126K/yr

This position reports to Executive Director, Medical Writing Oncology and is part of the Medical ... Primarily remote role with periodic on-site meetings in office. Must be able to travel domestically ...

Amiculum

Experienced medical writer - USA

Chicago, IL · On-site +1

... oncology and/or hematology. The role Our core expertise is developing accurate and engaging ... Remote and hybrid working options as standard * Continuous learning and professional development ...

Synterex

Senior Medical Writer

Princeton, NJ · Remote

Synterex offers remote or on-site services, with a focus on providing clear, concise, accurate, and ... Oncology, Infectious Disease, or Vaccine experience desired * Experience desired in writing ...

Telix Pharmaceuticals

Medical Writer

... oncology and rare diseases. See Yourself at Telix The Medical Writer will contribute to the ... We have hybrid and remote employees located all around the world. We offer competitive salaries ...

Veristat

... oncology projects in the past 5 years * 350+ rare disease projects delivered in the past 5 years ... Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ...

Revolution Medicines

Principal Medical Writer

Serves as medical writing lead on complex clinical regulatory documents, including protocols, IBs ... Experience with oncology therapeutics. * Familiarity with StartingPoint, EndNote, Veeva RIM, and ...

Veristat

... oncology projects in the past 5 years * 350+ rare disease projects delivered in the past 5 years ... Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ...

ApotheCom

Medical Writer

Yardley, PA · On-site +1

Medical Writer ApotheCom, an Inizio Medical company, is an exciting leader in the field of medical ... PTO This position is open to candidates who are looking for a fully remote or hybrid opportunity ...

Merck Group

Senior Principal Medical Writer

Billerica, MA · On-site +1

$126K - $215K/yr

No Department: HC-RD-RO Regulatory Oncology Recruiter: Sarah Ellis This information is for ... Vendor management and remote leadership * Strong communication, negotiation, and stakeholder ...

Merck Group

Senior Principal Medical Writer

Billerica, MA · On-site +1

$126K - $215K/yr

No Department: HC-RD-RO Regulatory Oncology Recruiter: Sarah Ellis This information is for ... Vendor management and remote leadership * Strong communication, negotiation, and stakeholder ...

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How much do remote oncology medical writer jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for remote oncology medical writer 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 remote oncology medical writer?

A Remote Oncology Medical Writer is a professional who creates scientific documents related to cancer research, treatments, and clinical trials, often working from a location outside of a traditional office setting. They translate complex medical data into clear, accurate materials such as manuscripts, regulatory documents, and educational content for healthcare professionals, regulatory agencies, or patients. This role requires strong writing skills, a background in life sciences, and specialized knowledge of oncology. Remote writers collaborate with researchers, clinicians, and pharmaceutical companies using digital communication tools. Their work helps ensure that critical oncology information is communicated effectively and accurately.

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

To thrive as a Remote Oncology Medical Writer, you need a strong background in life sciences or medicine, excellent written communication skills, and often an advanced degree such as an MSc or PhD. Familiarity with medical writing guidelines (e.g., ICH, GPP3), reference management tools, and document management systems is typically required. Attention to detail, time management, and the ability to synthesize complex data for diverse audiences are essential soft skills. These capabilities ensure the production of accurate, clear, and compliant oncology documents that support clinical research and regulatory submissions.

What are common challenges faced by remote oncology medical writers, and how can they be managed?

Remote Oncology Medical Writers often encounter challenges such as staying current with rapidly evolving cancer research, managing complex scientific information, and maintaining clear communication with multidisciplinary teams across different time zones. To address these challenges, it's important to cultivate strong organizational skills, regularly participate in relevant training or webinars, and utilize collaborative digital tools to streamline feedback and maintain alignment with team goals. Building a network with other remote writers and oncology professionals can also provide valuable support and resources.

Can you work from home as a remote oncology medical writer?

Yes, remote oncology medical writers typically work from home, as their role involves creating scientific content, reviewing medical literature, and collaborating with teams virtually. This position often requires strong writing skills, familiarity with medical software, and the ability to meet deadlines independently.
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Remote Oncology Medical Writer jobs near you
Infographic showing various Remote Oncology Medical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $96,235 per year, or $46.3 per hour.

Medical Writer / Clinical Document - Remote

YO AI Labs

Washington, DC • Remote

$50 - $80/hr

Full-time

Posted 24 days ago

Job description

Job Title: Medical Writer / Clinical Document Author

Location: Remote
Job Type: Contractor
Pay: $50–$80/hour

Job Overview

We are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing.

Key Responsibilities

  • Author and review Clinical Study Reports (CSRs) and other regulatory documents.

  • Interpret clinical protocols and ensure compliance with ICH guidelines.

  • Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.

  • Review safety documentation, including DSURs and PSURs/PBRERs.

  • Provide structured feedback and collaborate with cross-functional teams.

  • Support AI-assisted documentation evaluation and quality improvement initiatives.

Required Skills

  • Regulatory Medical Writing

  • Clinical Study Report (CSR) Authoring

  • ICH E3 Guidelines

  • Scientific Accuracy Assessment

  • Source Data Verification

  • Clinical Protocol Interpretation

  • TFL Analysis

  • eCTD Knowledge

  • Strong Written Communication & Collaboration

Qualifications

  • 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment.

  • Experience authoring Clinical Study Reports and regulatory documentation.

  • Strong knowledge of ICH E3, ICH E2F, ICH E2C, and eCTD requirements.

  • Advanced degree in Life Sciences, Pharmacy, Medicine, or a related field (MD, PharmD, PhD, or MSc).

  • Experience in oncology and haematology is preferred.