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Remote Medical Writer Jobs Near Me

Medasource

Lead Medical Writer

Dublin, OH · On-site

$80 - $90/hr

Lead Medical Writer Remote (must be based in EST) Compensation: $80-$90 per hour Contract Length: 2 month Contract to Hire (40 hours/week) Start Date: 7/1/26 ABOUT THE ROLE Our client is a global ...

Motorola

Technical Writer

Delaware, OH · On-site +1

$55K - $65K/yr

Medical, Dental, Visionbenefits * 401K with Company Match * 10 Paid Holidays * GenerousPaidTime Off Packages * Employee Stock Purchase Plan * PaidParental & Family Leave * and more! EEO Statement ...

Manifest Solutions

Technical Writer

Columbus, OH

Manifest Solutions is currently seeking a Senior Compliance Technical Writer for a position in Columbus, OH. * Prepare, edit, and maintain NERC compliance documentation, including: Procedures ...

Manifest Solutions

Technical Writer

Columbus, OH · On-site

Manifest Solutions is currently seeking a Senior Compliance Technical Writer for a position in Columbus, OH. * Prepare, edit, and maintain NERC compliance documentation, including: Procedures ...

VIVA USA INC

Technical Writer

Columbus, OH · On-site

Technical Writer (TW3) is needed for the Modernization / Re-write of a .NET Application. The TW3 would be responsible for all Technical Documentation, Business Process descriptions, system ...

Digitek Software, Inc.

Technical Writer

Columbus, OH · On-site

One of our clients is looking for the position of in Technical Writer based on following skills: Onsite 1. 1.Drafting of Administrative Technology Policies for the Department of Technology (60%) 2. 2.

VIVA USA INC

Technical Writer

Columbus, OH · On-site

... writing administrative / technology IT governance policies and procedure - Required - 4 Years Experience with researching market trends for public sector IT organizations - Required - 3 Years Notes:

IDEALFORCE LLC

Technical Writer (39831)

Columbus, OH · On-site

Strong communication skills: both written and spoken. Work with Application Team members to enhance their understanding of end-user and technical documentation. Ensure messages and terminology is ...

Info Origin Inc.

Technical Writer 3

Columbus, OH · On-site

Experience writing administrative / technology IT governance policies and procedure - Required 4 Years * Experience with researching market trends for public sector IT organizations - Required 3 ...

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How much do remote medical writer jobs pay per hour?

As of Aug 2, 2026, the average hourly pay for remote medical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.
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Remote Medical Writer jobs near you
A map of the United States highlighting the number of Remote Medical Writer job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Remote Medical Writer job openings in each state, with California having the most at 2 and Hawaii the least at 0.

Lead Medical Writer

Medasource

Dublin, OH • On-site

$80 - $90/hr

Contractor

Re-posted 12 days ago

Job description

Lead Medical Writer
Remote (must be based in EST)
Compensation: $80-$90 per hour
Contract Length: 2 month Contract to Hire (40 hours/week)
Start Date: 7/1/26
ABOUT THE ROLE
Our client is a global healthcare services and products company providing pharmaceuticals, medical products, and supply chain solutions to hospitals, pharmacies, and healthcare providers. The organization plays a critical role in helping healthcare systems improve efficiency, reduce costs, and enhance patient care through integrated distribution and data-driven solutions. As a Lead Medical Writer on a 2-month remote contract, you will autonomously author and review a range of clinical regulatory documents, including CTD Module II summaries, Clinical Overviews, Clinical Study Reports (CSRs), and responses to health authority queries. You will contribute scientifically and strategically to submission teams, plan data analyses, review statistical analysis plans, and collaborate with cross-functional stakeholders such as Clinical Sciences, Clinical Pharmacology, Biometry, Drug Safety, Clinical Operations, CMC, and Regulatory Affairs. This role requires advanced medical writing skills, deep knowledge of regulatory requirements, the ability to mentor junior writers, and strong interpersonal and presentation abilities. Candidates must be available to work in the Eastern Standard Time zone.
WHAT YOU'LL DO
  • Autonomously write and review clinical regulatory documents, including CTD Module II summaries, Clinical Overviews, Clinical Study Reports (CSRs), and other regulatory submissions such as responses to health authority questions, briefing books, 120-day safety updates, pediatric investigational plans, and investigator brochures
  • Contribute scientifically and strategically to submission teams at the project and/or study team level, providing input on pooling strategy, content expertise, and guidance on regulatory requirements
  • Plan and review data analyses and presentations for CSRs; review statistical analysis plans and related documents
  • Collaborate effectively with cross-functional stakeholders, including Clinical Sciences, Clinical Pharmacology, Biometry, Drug Safety, Clinical Operations, CMC, and Regulatory Affairs
  • Work with in-house Documentation Specialists to produce high-quality final documents and ensure timely delivery
  • Mentor and develop junior medical writers, providing guidance and support as needed
  • Demonstrate advanced medical writing skills and maintain up-to-date knowledge of regulatory document requirements and guidelines
  • Work independently and as part of a team, managing multiple priorities and meeting challenging deadlines
  • Exhibit excellent interpersonal and presentation skills in all interactions
  • Maintain advanced proficiency in English for all written and verbal communications
WHAT YOU BRING
  • Advanced degree in life sciences (PhD, PharmD, MD, or MS preferred)
  • 5+ years of regulatory/medical writing experience in the pharmaceutical industry across several therapeutic areas
  • Proven ability to autonomously write and review clinical regulatory documents (e.g., CTD Module II summaries, CSRs, Clinical Overviews, Investigator brochures, and other regulatory submissions)
  • Strong knowledge of regulatory document requirements and guidelines
  • Experience contributing scientifically and strategically to submission teams
  • Ability to plan data analyses and review statistical analysis plans for CSRs
  • Excellent collaboration skills with cross-functional stakeholders
  • Well-developed medical writing skills with attention to quality and deadlines
  • Ability to mentor and develop junior medical writers
  • Ability to work independently and as part of a team
  • Strong interpersonal and presentation skills
  • Advanced level of English proficiency
  • Ability to work under pressure and meet challenging deadlines
  • Remote work capability with availability in Eastern Standard Time (EST)

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