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Clinical Medical Writer Editor Jobs (NOW HIRING)

labconnect

Medical Writer

The Medical Writer is responsible for authoring clinical trial and regulatory documents, through ... Advanced knowledge of scientific/technical writing and editing. * Strong time and project ...

Telix Pharmaceuticals

Medical Writer

This role will provide medical writing support by organizing, analyzing, and interpreting ... and editing of high-quality regulatory documents and reports (primarily clinically oriented ...

Gritter Francona

Technical Writer/Editor

Virginia, IL · On-site

The Technical Writer/Editor produces clear, digital resources by gathering and translating ... Health Care Plan (Medical, Dental & Vision) * Retirement Plan (401k, IRA) * Life Insurance (Basic ...

Node.Digital

Technical Writer & Editor

Arlington, TX · On-site

Technical Writer & Editor Location: Arlington, VA Must have an active Top Secret Clearance Must be ... Medical * Dental * Vision * Basic Life * Health Saving Account * 401K * Three weeks of PTO * 10 ...

Adecco

Sr Med Writer

Morrisville, NC · Remote

$72.90 - $81/hr

... clinical development, preclinical research, therapeutic areas, or regulatory submissions. Skills & Competencies * Excellent medical writing, editing, proofreading, and data interpretation skills.

Hive Group LLC

Tech Writer / Editor

Petersburg, VA · On-site

We are seeking a highly skilled Technical Writer/Editor to support the US Army Combined Arms ... medical, dental, vision), life and disability insurance, retirement contributions, paid leave ...

Applied Underwriters

Writer/Editor

Omaha, NE · On-site

Proficiency in Associated Press writing style; and understanding of SEO, GEO and UX writing best practices Our Benefits Include: * 100% employer-paid medical, dental, and vision insurance for ...

Icon plc

Principal Medical Writer ICON is a global healthcare intelligence and clinical research ... for clinical writing * Exceptional writing and editing skills, with a keen eye for detail and ...

ICON

Principal Medical Writer

Blue Bell, PA · On-site +1

Principal Medical Writer ICON is a global healthcare intelligence and clinical research ... for clinical writing * Exceptional writing and editing skills, with a keen eye for detail and ...

Icon plc

Principal Medical Writer

Blue Bell, PA · On-site

Principal Medical Writer ICON is a global healthcare intelligence and clinical research ... for clinical writing * Exceptional writing and editing skills, with a keen eye for detail and ...

Applied Underwriters

Writer/Editor

Omaha, NE · On-site

Proficiency in Associated Press writing style; and understanding of SEO, GEO and UX writing best practices Our Benefits Include: * 100% employer-paid medical, dental, and vision insurance for ...

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Showing results 21-40

All JobsClinical Medical Writer Editor Jobs

Clinical Medical Writer Editor information

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$37K

$84.5K

$130K

How much do clinical medical writer editor jobs pay per year?

As of Sep 10, 2026, the average yearly pay for clinical medical writer editor in the United States is $84,537.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,000.00 and $101,500.00 per year, depending on experience, location, and employer.

What are popular job titles related to Clinical Medical Writer Editor jobs?

For Clinical Medical Writer Editor jobs, the most frequently searched job titles are:

Infographic showing various Clinical Medical Writer Editor job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, and 4% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $84,537 per year, or $40.6 per hour.

Medical Writer

Remote

labconnect
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about labconnectexternal

Full-time

Re-posted 25 days ago

Job description

The Medical Writer is responsible for authoring clinical trial and regulatory documents, through independent assignment and oversight as well as engagement within a cross-functional team dynamic. This role requires strategic thinking with exceptional scientific and technical writing skills, excellent communication skills and attention to detail, and the ability to manage and prioritize project load independently.

Essential Duties and Responsibilities

  • Perform all document authoring steps as outlined by document type and template:
  • Author clinical trial and regulatory documents.
  • Coordinate quality control of clinical trial and regulatory documents.
  • Engage with cross-functional team, as needed.
  • Develop accurate, clear and compliant documents as per the project and regulatory requirements.

Education and Experience

  • Master’s Degree or above and at least 5 years’ experience in medical writing in the Biotech/Pharmaceutical industry OR Bachelor’s degree and at least 8 years’ experience in medical writing in the Biotech/Pharmaceutical industry.
  • Experience understanding and interpreting data/information and its practical application.

Skills and Ability

  • Excellent written/oral communication skills and attention to detail.
  • Advanced knowledge of scientific/technical writing and editing.
  • Strong time and project management skills.
  • Strong leadership experience in a team environment.
  • Ability to independently prioritize and execute projects in alignment with critical deadlines.
  • Industry experience required.

Supervisory Responsibilities: None

Physical Demands:

While performing the duties of this job, the occupant is regularly required to:

  • Prolonged periods of sitting at a desk and working on a computer.
  • Prolonged use of computer and headphones for conference calls.
  • Communicate effectively via phone, video, and email.
  • Use hands and fingers to operate a computer and other office equipment.

Travel Requirements: Minimal

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