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Contract Medical Writer Jobs in Raleigh, NC (NOW HIRING)

Adecco

Sr Med Writer

Morrisville, NC · Remote

$72.90 - $81/hr

Support program management activities, including timelines, budgets, forecasts, and contract ... Medical writing certifications such as AMWA, EMWA, or RAC are advantageous. * Strong understanding ...

Posted today

IQVIA

Site Contract Manager

Durham, NC · On-site

$86K - $115K/yr

Strong legal, financial and/or technical writing skills. * Strong understanding of regulated ... innovative medical treatments to help improve patient outcomes and population health worldwide.

IQVIA, Inc.

Site Contract Manager

Durham, NC · On-site

$86K - $115K/yr

Strong legal, financial and/or technical writing skills. * Strong understanding of regulated ... innovative medical treatments to help improve patient outcomes and population health worldwide.

IQVIA

Site Contract Manager

Durham, NC · On-site

$86K - $115K/yr

Strong legal, financial and/or technical writing skills. * Strong understanding of regulated ... innovative medical treatments to help improve patient outcomes and population health worldwide.

IQVIA

FSP Contract Negotiator

Durham, NC · On-site

Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical ... innovative medical treatments to help improve patient outcomes and population health worldwide.

IQVIA, Inc.

FSP Contract Negotiator

Durham, NC · On-site

... writing skills. • Strong understanding of regulated clinical trial environment and knowledge of ... innovative medical treatments to help improve patient outcomes and population health worldwide.

Veolia

Commercial Contracts Manager

Cary, NC · On-site

$110 - $118/hr

Prepare persuasive positions for (and sometimes lead) complex contract negotiations for dispute ... Good verbal and written communications skills, including presentations to customers and Veolia team ...

Veolia

Commercial Contracts Manager

Cary, NC · On-site

Prepare persuasive positions for (and sometimes lead) complex contract negotiations for dispute ... Good verbal and written communications skills, including presentations to customers and Veolia team ...

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

Contract Medical Writer information

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How much do contract medical writer jobs pay per hour?

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

A Contract Medical Writer is a professional who creates scientific documents on a freelance or contract basis for pharmaceutical, biotech, or healthcare companies. They develop clinical study reports, regulatory submissions, manuscripts, and other medical content. Unlike full-time employees, contract medical writers work on a project-by-project basis, often remotely. They must have strong writing skills, scientific knowledge, and an understanding of medical regulations. This role offers flexibility but requires self-discipline and deadline management.

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

To thrive as a Contract Medical Writer, you need a thorough understanding of scientific concepts, excellent writing skills, and often an advanced degree in life sciences or a related field. Familiarity with regulatory documentation formats (such as ICH, FDA, or EMA standards), medical journal requirements, and tools like Microsoft Office Suite or referencing software is vital. Strong organizational skills, attention to detail, and the ability to communicate complex information clearly are essential soft skills. These capabilities ensure accuracy, compliance, and the effective communication of scientific data to diverse audiences in the healthcare industry.

What types of projects can I expect to work on as a contract medical writer?

As a Contract Medical Writer, you may work on a variety of projects including clinical trial protocols, regulatory submissions, scientific manuscripts, patient education materials, and medical communications for conferences or publications. The work is typically project-based, with deadlines and deliverables defined by clients or pharmaceutical companies. You will often collaborate remotely with clinical researchers, regulatory teams, and subject matter experts to gather information and ensure accuracy. This diversity of projects keeps the role dynamic and allows for continuous learning in different therapeutic areas or document types.

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

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

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

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

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

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

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

Contract Medical Writer jobs near you
Infographic showing various Contract Medical Writer job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, and 5% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% 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 14 hours ago

Posted today

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.