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Document Writer Jobs in Raleigh, NC (NOW HIRING)

IQVIA, Inc.

Principal Medical Writer

Durham, NC · On-site

This role plays a critical part in ensuring that documents such as Investigator's Brochures (IBs ... The successful candidate will act as a lead writer for key summary documents , providing strategic ...

IQVIA

Principal Medical Writer

Durham, NC

This role plays a critical part in ensuring that documents such as Investigator's Brochures (IBs ... The successful candidate will act as a lead writer for key summary documents , providing strategic ...

Ask IT consulting

Test Scripts Writer

Durham, NC

$28/hr

NC FAST P4 Test Scripts Writer Location : Research Triangle Park, Durham, NC REQ ID: 496061 ... Documents, developing requirements into test conditions, cases and scripts, development and ...

Infojini Inc

Test Scripts Writer

Durham, NC

$30/hr

Test Scripts Writer Location: Durham, NC 27709 Duration: 12+ months contract Rate:$30/hr on C2C ... Documents, developing requirements into test conditions, cases and scripts, development and ...

GlaxoSmithKline

Principal Medical Writer

Durham, NC · Remote

Lead authoring and strategic planning for clinical and regulatory documents, including protocols, clinical study reports, briefing documents, and submission dossiers. * Manage end-to-end writing ...

US IT Solutions Inc

Test Scripts Writer

Durham, NC

Test Scripts Writer Duration 12 Months Location: Durham, NC Description: Duties include analyzing ... Documents, developing requirements into test conditions, cases and scripts, development and ...

GSK

Principal Medical Writer

Durham, NC · On-site

Lead authoring and strategic planning for clinical and regulatory documents, including protocols, clinical study reports, briefing documents, and submission dossiers. * Manage end-to-end writing ...

MMS

Nonclinical Writer

Raleigh, NC · On-site

Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, Investigator's Brochure [IB], Nonclinical Study Reports, Meeting Requests ...

ViiV Healthcare

Principal Medical Writer

Durham, NC · On-site

Lead authoring and strategic planning for clinical and regulatory documents, including protocols, clinical study reports, briefing documents, and submission dossiers. * Manage end-to-end writing ...

ViiV Healthcare

Principal Medical Writer

Durham, NC · Remote

Lead authoring and strategic planning for clinical and regulatory documents, including protocols, clinical study reports, briefing documents, and submission dossiers. * Manage end-to-end writing ...

Infojini Inc

Technical Writer(locals only)

Raleigh, NC · On-site

They are seeking a Technical Writer in Raleigh, NC to create and manage technical documentation for an IT audience. Responsibilities : • Demonstrated experience writing technical documentation for ...

Infojini Inc

Test script writer

Raleigh, NC · On-site

... technical documentation and training materials using various Microsoft Office tools ... Responsibilities : • The technical writer will be expected to heavily use the Microsoft Office ...

Kelly Services

Contract Technical Writer

Raleigh, NC

$40 - $47/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Ensure all documents comply with cGMP requirements and internal quality systems. * Track assigned ... Strong technical writing skills with an emphasis on clarity, consistency, and regulatory compliance.

Infojini Inc

Sr. Technical Writer

Raleigh, NC

We offer an excellent compensation package We are looking for Sr. Technical Writer in Raleigh, NC ... Documented experience in developing IT Operational processes and Procedure * Experience meeting ...

Elite Workforce Inc

APD Writer at NC

Raleigh, NC · On-site

State of North Carolina Duration: 12+ Months We're seeking an experienced APD Writer to develop MES Advanced Planning Documents (APDs) and related materials for a Medicaid program. The role focuses ...

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Showing results 21-40

All JobsDocument Writer JobsDocument Writer Jobs in Raleigh, NC

Document Writer information

See Raleigh, NC salary details

$20

$34

$52

How much do document writer jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for document writer in Raleigh, NC is $34.98, according to ZipRecruiter salary data. Most workers in this role earn between $23.37 and $48.61 per hour, depending on experience, location, and employer.

What does a document writer do?

A Document Writer is responsible for creating, editing, and formatting various types of documents such as reports, manuals, proposals, and business correspondence. They ensure that documents are clear, well-organized, and tailored to the intended audience. Document Writers often work closely with subject matter experts to gather information and may use specialized software to maintain consistency and quality. Their role is essential in ensuring effective communication within an organization.

What are some common challenges faced by document writers when working with subject matter experts (SMEs)?

Document Writers often collaborate closely with subject matter experts to gather accurate information, but a common challenge is translating complex or technical details into clear, accessible documentation for the intended audience. SMEs may use specialized jargon or provide dense information, so Document Writers need strong communication skills to clarify requirements and ensure nothing is lost in translation. Building rapport and maintaining regular communication with SMEs can help streamline the process and lead to more effective, user-friendly documents.

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

To thrive as a Document Writer, you need excellent written communication skills, attention to detail, and proficiency in language usage, typically supported by a relevant degree or experience in writing or communications. Familiarity with word processing software, document management systems, and sometimes industry-specific tools like Adobe Acrobat or content management systems is common. Strong research abilities, time management, and adaptability help Document Writers effectively convey complex information and meet deadlines. These skills ensure documents are accurate, clear, and tailored to their intended audience, which is essential for effective communication and organizational success.

Are there remote document writing jobs?

Yes, many document writer positions are available as remote jobs, especially in fields like technical writing, content creation, and editing. These roles often require strong writing skills, familiarity with tools like Microsoft Word or Google Docs, and the ability to work independently on flexible schedules.

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

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

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

The top searched job categories for Document Writer jobs in Raleigh, NC are:

Document Writer jobs near you
Infographic showing various Document Writer job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 13% Part Time, 1% Temporary, and 8% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $72,753 per year, or $35 per hour.

Principal Medical Writer

IQVIA, Inc.

Durham, NC • On-site

Full-time

Posted 10 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 224 rated it services

Job description

Overview
We are seeking an experienced PrincipalMedical Writer to lead the development of high-quality clinical and regulatory documents supporting global regulatory submissions. This role plays a critical part in ensuring that documents such as Investigator's Brochures (IBs), Clinical Study Reports (CSRs), and Module II summaries that are scientifically accurate, consistent, and aligned with program objectives and global regulatory requirements.
The successful candidate will act as a lead writer for key summary documents, providing strategic guidance to cross-functional teams while overseeing medical writing activities across multiple compounds. This position reports to the Director of Medical Writing (or above).
Key Responsibilities
  • Lead the development of high-quality clinical and regulatory documents (e.g., Investigator's Brochures, Clinical Study Reports, clinical summaries, and marketing authorization submissions) in compliance with global regulatory guidelines (ICH, FDA, EMA) and internal standards
  • Serve as the lead writer for key summary documents, overseeing medical writing activities across multiple compounds or programs
  • Provide strategic guidance to cross-functional teams on document content, messaging, and regulatory positioning to ensure alignment with program goals
  • Manage medical writing projects, including planning, timelines, resource coordination, and delivery to ensure milestones and submission deadlines are met
  • Collaborate with cross-functional stakeholders (Clinical, Regulatory Affairs, Biostatistics, Safety, etc.) to gather, interpret, and accurately present clinical data
  • Mentor and support other medical writers, ensuring high-quality, scientifically sound, and consistent deliverables across projects
  • Review and edit project-related documents to ensure accuracy, clarity, consistency, and compliance with templates and style guides
  • Attend project and team meetings to provide expert input on document development, study data interpretation, and process improvements
  • Contribute to and lead process improvement initiatives to enhance efficiency, quality, and consistency in document preparation
  • Develop, maintain, and refine standard operating procedures (SOPs), templates, and best practices for medical writing
  • Stay current with evolving global regulatory requirements, industry trends, and therapeutic area knowledge to ensure compliance and innovation

Qualifications
  • Bachelor's degree in a scientific, clinical, regulatory, or related field required; advanced degree (e.g., MSc, PhD, PharmD, MD) preferred
  • Minimum of 7+ years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or preclinical development will also be considered
  • Strong knowledge of global regulatory requirements and guidelines (e.g., ICH, FDA, EMA) across all phases of clinical development
  • Broad understanding of clinical research processes, including study design, data analysis, and regulatory submission requirements
  • Demonstrated ability to lead writing activities for complex documents and provide strategic input to cross-functional teams
  • Excellent written and verbal communication skills, with the ability to clearly and accurately present complex scientific and clinical information
  • Strong organizational, time management, and project management skills, with the ability to manage multiple priorities and meet tight deadlines
  • Proven ability to work collaboratively in a cross-functional, team-oriented environment while also operating independently when needed
  • High attention to detail with a commitment to quality, consistency, and scientific accuracy
  • Proficiency in Microsoft Word and document formatting best practices

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $84,400.00 - $211,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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