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Remote Contract Medical Writer Jobs in Raleigh, NC

Adecco

Sr Med Writer

Morrisville, NC · Remote

$72.90 - $81/hr

Remote Pay Rate: $72.90-$81.00/hour Schedule: Monday-Friday, 8:00 AM-5:00 PM Hours: Target of 40 ... Support program management activities, including timelines, budgets, forecasts, and contract ...

New

GlaxoSmithKline

Principal Medical Writer

Durham, NC · Remote

Experience working in multicultural or remote team settings. * Proven ability to independently ... Medical Writing, Pharmaceutical Industry, Presentation Techniques, Regulatory Submissions ...

ViiV Healthcare

Principal Medical Writer

Durham, NC · Remote

Experience working in multicultural or remote team settings. * Proven ability to independently ... Medical Writing, Pharmaceutical Industry, Presentation Techniques, Regulatory Submissions ...

micro1 AI

Medical Writing Manager

Cary, NC · Remote

$50 - $80/hr

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 ...

micro1 AI

Medical Writing Manager

Raleigh, NC · Remote

$50 - $80/hr

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 ...

micro1 AI

Medical Writing Manager

Durham, NC · Remote

$50 - $80/hr

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 ...

micro1 AI

Medical Billing Specialist

Raleigh, NC · Remote

$50 - $80/hr

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 ...

micro1 AI

Medical Billing Specialist

Durham, NC · Remote

$50 - $80/hr

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 ...

micro1 AI

Medical Billing Specialist

Cary, NC · Remote

$50 - $80/hr

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 ...

Ascent Placement Partners

Be Seen First

Remote Software Engineer - Technical Advisor

Durham, NC · Remote

$150/hr

This is a 6 month, W2 , contract opportunity, with the chance of extension. This mostly ... Writing clear, original technical rationales explaining code failures (all written work must be ...

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All JobsContract Medical Writer JobsRemote Contract Medical Writer JobsRemote Contract Medical Writer Jobs in Raleigh, NC

Remote Contract Medical Writer information

See Raleigh, NC salary details

$13

$37

$56

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

As of Sep 7, 2026, the average hourly pay for remote contract medical writer in Raleigh, NC is $37.56, according to ZipRecruiter salary data. Most workers in this role earn between $25.48 and $47.45 per hour, depending on experience, location, and employer.

What is a remote contract medical writer?

A Remote Contract Medical Writer is a professional who creates scientific documents, such as clinical study reports, regulatory submissions, or educational materials, for pharmaceutical, biotech, or healthcare organizations while working remotely on a contract basis. They translate complex medical data into clear, accurate, and compliant content tailored to the target audience, such as regulatory agencies, healthcare providers, or patients. These writers typically collaborate with subject matter experts, researchers, and regulatory teams, and their work often follows strict industry guidelines and deadlines. Remote contract roles offer flexibility and the ability to work with multiple clients from different locations.

What are the key skills and qualifications needed to thrive as a remote contract medical writer, and why are they important?

To thrive as a Remote Contract Medical Writer, you need a strong background in life sciences, excellent research abilities, and proven writing skills, often supported by a relevant degree or advanced certification. Familiarity with regulatory documentation, referencing software (such as EndNote), and platforms like Microsoft Office or document management systems is typically required. Keen attention to detail, time management, and clear communication are essential soft skills for meeting deadlines and collaborating remotely. These skills ensure the creation of accurate, compliant, and high-quality medical documents for clients and regulatory agencies.

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

Remote contract medical writers often encounter challenges such as managing multiple deadlines for different clients, adapting to varying writing styles and guidelines, and maintaining clear communication across virtual teams. To address these, it’s important to develop strong organizational skills, set clear expectations with clients, and utilize project management tools. Regular check-ins and proactive communication with clients and collaborators help ensure alignment and smooth workflow.

What is the difference between Remote Contract Medical Writer vs Remote Full-Time Medical Writer?

AspectRemote Contract Medical WriterRemote Full-Time Medical Writer
CredentialsTypically requires medical or scientific degrees, writing experience, and industry certificationsSame as contract; often requires similar credentials and certifications
Work EnvironmentProject-based, flexible hours, short-term engagementsPermanent employment, consistent schedule, ongoing projects
Employer & Industry UsageFreelance or consulting firms, biotech, pharma companiesPharmaceutical companies, CROs, biotech firms
Search & Comparison IntentHigh overlap in skills, project scope, and industry contextSimilar roles with different employment types

The main difference between a Remote Contract Medical Writer and a Remote Full-Time Medical Writer lies in employment type and engagement duration. Contract writers work on specific projects with flexible hours, while full-time writers have ongoing employment with consistent schedules. Both roles require similar credentials and industry experience, making them comparable in skills and responsibilities.

What are the most commonly searched types of Remote Medical Writer jobs in Raleigh, NC?

The most popular types of Remote Medical Writer jobs in Raleigh, NC are:

What are popular job titles related to Remote Contract Medical Writer jobs in Raleigh, NC?

For Remote Contract Medical Writer jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Remote Contract Medical Writer jobs in Raleigh, NC look for?

The top searched job categories for Remote Contract Medical Writer jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Remote Contract Medical Writer jobs?

Cities near Raleigh, NC with the most Remote Contract Medical Writer job openings:

Remote Contract Medical Writer jobs near you
Infographic showing various Remote Contract Medical Writer job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $78,120 per year, or $37.6 per hour.

Sr Med Writer

Adecco

Morrisville, NC • Remote

$72.90 - $81/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New

Job description

Senior Medical Writer

Location: Remote
Pay Rate: $72.90–$81.00/hour
Schedule: Monday–Friday, 8:00 AM–5:00 PM
Hours: Target of 40 hours/week; hours may vary based on workload
Preference: East Coast candidates preferred

Position Summary

We are seeking an experienced Senior Medical Writer to provide high-quality regulatory medical and scientific writing support for Phase 1–3 clinical development programs involving pharmaceutical and biologic products.

The ideal candidate will bring strong medical writing expertise, therapeutic area knowledge, and a solid understanding of clinical development and global regulatory requirements. This role works closely with internal and external stakeholders to develop high-quality regulatory documents and ensure timely delivery.

Key Responsibilities

  • Serve as a primary author for regulatory documents supporting Phase 1–3 clinical development, including clinical study protocols, protocol amendments, and Clinical Study Reports (CSRs).

  • Research, author, and edit complex clinical, scientific, and regulatory documents, including Investigator’s Brochures (IBs), IND documents, and MAA documents.

  • Review documents prepared by junior writers and peers and provide constructive feedback.

  • Mentor and train junior medical writers on document development, regulatory requirements, processes, and therapeutic area knowledge.

  • Ensure documents meet applicable quality standards, regulatory requirements, and client-specific expectations.

  • Develop and implement best practices to improve document quality, efficiency, and delivery.

  • Support program management activities, including timelines, budgets, forecasts, and contract modifications, as needed.

  • Identify and address scope changes and out-of-scope activities.

  • Use appropriate AI and technology-enabled tools to improve the efficiency and quality of document development while following applicable policies and client requirements.

  • Manage multiple priorities in a fast-paced environment while meeting critical client and regulatory submission timelines.

  • Deliver high-quality work within established timelines, budgets, and client expectations.

Qualifications

  • Bachelor’s degree in a scientific discipline or equivalent relevant education and experience; advanced degree preferred.

  • 5+ years of relevant experience in medical writing or a comparable field.

  • Pharmaceutical or CRO industry experience preferred.

  • Medical writing certifications such as AMWA, EMWA, or RAC are advantageous.

  • Strong understanding of global, regional, and national regulatory and document development guidelines.

  • In-depth knowledge of at least one specialty area, such as clinical development, preclinical research, therapeutic areas, or regulatory submissions.

Skills & Competencies

  • Excellent medical writing, editing, proofreading, and data interpretation skills.

  • Strong project management and organizational abilities.

  • Excellent written, verbal, and presentation skills.

  • Strong interpersonal, problem-solving, negotiation, and decision-making skills.

  • Exceptional attention to detail and quality.

  • Ability to work independently while collaborating effectively with cross-functional and external teams.

  • Strong computer skills, including Microsoft Office, Excel, Outlook, client templates, and document management systems.

  • Ability to adapt to changing priorities and work effectively under tight deadlines.

Work Schedule

This is a fully remote position, Monday through Friday, generally 8:00 AM–5:00 PM. The target schedule is approximately 40 hours per week, although hours may vary depending on workload and business needs.

East Coast candidates are preferred.


Pay Details: $72.90 to $81.00 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
Military connected talent encouraged to apply
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.adecco.com/en-us/candidate-privacy
The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
  • The California Fair Chance Act
  • Los Angeles City Fair Chance Ordinance
  • Los Angeles County Fair Chance Ordinance for Employers
  • San Francisco Fair Chance Ordinance

Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.