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Medical Writer Jobs in Raleigh, NC (NOW HIRING)

IQVIA, Inc.

Senior Medical Writer

Durham, NC · On-site

Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the ...

IQVIA

Senior Medical Writer

Durham, NC

Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the ...

IQVIA, Inc.

Senior Medical Writer

Durham, NC · On-site

Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the ...

IQVIA

Senior Medical Writer

Durham, NC

Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the ...

IQVIA

Senior Medical Writer

Durham, NC · On-site

Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the ...

GlaxoSmithKline

Principal Medical Writer

Durham, NC · On-site +1

ViiV Healthcare is seeking a Principal Medical Writer who will lead and deliver high-quality medical writing for complex clinical and regulatory projects. You will work closely with clinical ...

ViiV Healthcare

Principal Medical Writer

Durham, NC · On-site +1

ViiV Healthcare is seeking a Principal Medical Writer who will lead and deliver high-quality medical writing for complex clinical and regulatory projects. You will work closely with clinical ...

GSK

Principal Medical Writer

Durham, NC · On-site

ViiV Healthcare is seeking a Principal Medical Writer who will lead and deliver high-quality medical writing for complex clinical and regulatory projects. You will work closely with clinical ...

ViiV Healthcare

Principal Medical Writer

Durham, NC · On-site

ViiV Healthcare is seeking a Principal Medical Writer who will lead and deliver high-quality medical writing for complex clinical and regulatory projects. You will work closely with clinical ...

MMS

Senior Medical Writer (Remote)

Raleigh, NC · On-site

Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical ...

Trilogy

Senior/Principal Medical Writer - USA

Durham, NC · On-site +1

$120K - $159K/yr

Trilogy Writing & Consulting,anIndegeneCompany, ishiring Senior/Principal Medical Writers (USA) to support our growing company in producing regulatory documentation for the international ...

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All JobsMedical Writer JobsMedical Writer Jobs in Raleigh, NC

Medical Writer information

See Raleigh, NC salary details

$11

$44

$76

How much do medical writer jobs pay per hour?

As of Jul 2, 2026, the average hourly pay for medical writer in Raleigh, NC is $44.97, according to ZipRecruiter salary data. Most workers in this role earn between $32.69 and $54.42 per hour, depending on experience, location, and employer.

Do you need a PhD to be a Medical Writer?

A PhD is not required to become a Medical Writer, but many professionals in the field hold advanced degrees such as a master's or doctorate. Strong writing skills, a background in life sciences or healthcare, and familiarity with scientific literature are essential for success in this role.

What are medical writers?

Medical writers are professionals who create scientific documents related to healthcare, medicine, and the life sciences. They produce materials such as clinical study reports, journal articles, regulatory submissions, and educational content for healthcare professionals or the public. Medical writers must have a strong understanding of medical terminology, research methods, and regulatory guidelines. Their work helps communicate complex scientific information clearly, accurately, and in compliance with industry standards.

Do medical writers make good money?

Medical writers typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions may start around $60,000 annually, while experienced professionals can earn over $100,000, especially with specialized knowledge or certifications. The role often involves working with scientific data, regulatory documents, and medical publications.

What Is the Job of a Medical Writer?

Medical writers create scientific documents and articles. This can include a variety of different types of papers, including research documents, educational or promotional literature, articles, and abstracts. You may ghostwrite for well-known physicians and scientists, or you may write under your own name, depending on what field you are in. Other medical writer jobs include journalists for medical magazines, authors of books, and those who write marketing materials for health care organizations. Regardless of your specialty, you must be able to interpret complex scientific information and create articles that people can read and understand, particularly when writing for the general public.

What is a Medical Writer?

A medical writer is a professional who creates scientific and medical documents such as research articles, regulatory submissions, and clinical trial reports. They combine expertise in medicine or life sciences with strong writing skills to communicate complex information clearly and accurately, often working in pharmaceutical, biotech, or healthcare industries.

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

To thrive as a Medical Writer, you need a strong background in life sciences or medicine, excellent written communication skills, and often an advanced degree such as a PhD, MD, or relevant certification. Familiarity with reference management software, medical literature databases, and regulatory guidelines like ICH or GPP is typically required. Attention to detail, the ability to interpret complex data, and collaboration skills set standout professionals apart in this role. These competencies ensure the production of accurate, compliant, and accessible medical documents crucial for regulatory approval, education, and communication in healthcare.

What is the difference between Medical Writer vs Clinical Writer?

AspectMedical WriterClinical Writer
CredentialsTypically requires a degree in life sciences, healthcare, or related fields; certifications like AMWA or EMWA are commonSimilar credentials; often holds degrees in life sciences with certifications in clinical research or writing
Work EnvironmentWorks in pharmaceutical, biotech, or healthcare companies, often in offices or remote settingsPrimarily in clinical research organizations, pharmaceutical companies, or hospitals, often in office or remote settings
Industry UsageUsed across pharma, biotech, medical device industries for regulatory, educational, and promotional contentFocused on clinical trial documentation, protocols, and reports within clinical research

Medical Writers and Clinical Writers share similar backgrounds and work environments, often collaborating in healthcare and pharmaceutical sectors. The main difference lies in their focus: Medical Writers create a broad range of medical content, while Clinical Writers specialize in clinical trial documentation and reports.

How do I become a Medical Writer?

To become a medical writer, typically a bachelor's degree in life sciences, healthcare, or a related field is required, often supplemented by advanced degrees or certifications in medical writing or regulatory writing. Gaining experience through internships, developing strong writing skills, and becoming familiar with industry guidelines and tools like reference management software can improve job prospects.

How does a Medical Writer typically collaborate with subject matter experts during a project?

Medical Writers frequently work closely with physicians, researchers, and regulatory specialists to ensure content accuracy and clarity. This collaboration often involves conducting interviews, reviewing scientific data, and incorporating expert feedback into drafts. Building strong professional relationships and maintaining clear communication are key for efficiently resolving technical questions and aligning final documents with project objectives. This teamwork is essential for producing high-quality, compliant materials that meet both scientific and regulatory standards.
More about Medical Writer jobs
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 Medical Writer jobs in Raleigh, NC? For Medical Writer jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Medical Writer jobs in Raleigh, NC look for? The top searched job categories for Medical Writer jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Medical Writer jobs? Cities near Raleigh, NC with the most Medical Writer job openings:
Medical Writer jobs near you
Infographic showing various Medical Writer job openings in Raleigh, NC as of June 2026, with employment types broken down into 75% Full Time, 15% Part Time, and 10% Contract. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $93,543 per year, or $45 per hour.
Senior Medical Writer

Senior Medical Writer

IQVIA, Inc.

Durham, NC • On-site

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

53rd of 207 rated it services

Job description

Job Overview:
Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs Senior Review of straightforward medical writing deliverables. Negotiates timelines and discusses/resolves customer comments.
Provides written and verbal feedback to junior staff, and to customers when appropriate.
Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or technical writing.
Essential Functions:
  • Take a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating and adhering to timelines, organizing document reviews, communicating directly with the customer.
  • Plan and organize workload for assigned projects and tasks: identify project needs, track timelines and implement customer requests.
  • Lead meetings on more challenging topics independently.
  • May present on standard Medical Writing processes at full-service bid defense meetings.
  • Assist in the training and development of junior staff, either formally as an assigned mentor or ad hoc for local colleagues or others. May develop and deliver training to the global team on a topic he/she has specific expertise in. May input into and deliver presentations on Medical Writing to other IQVIA groups.
  • May act as Project Manager for a more complex but single Medical Writing project which includes Project Finance/Invoicing responsibilities.
  • Complete project finance activities, including monitoring and forecasting budgeted hours.
  • Propose, review and approve budgets and costings for routine projects, including estimation of hours needed for Medical Writing tasks.
  • May take on a small customer lead role or assist an established partnership lead in their role.
  • May represent region or site on a Medical Writing initiative or cross-functional initiative.
  • Facilitates and brainstorms the identification of new ideas. May represent Medical Writing at a general capabilities audit.

Qualifications:
  • Bachelor's Degree Bachelor's Degree in life sciences related discipline or related field Required
  • Master's Degree Master's Degree in life sciences related discipline or related field Preferred
  • Ph.D. Ph.D. in life sciences related discipline or related field Preferred
  • Typically requires at least 5 years of highly relevant experience and related competency levels.
  • In-depth knowledge of the structural and content requirements of clinical study reports, protocols, and similar documents and ability to identify deficiencies, errors, and inconsistencies in a protocol or report.
  • Good understanding of common statistical methods used in clinical trials and/or interpretation of their results.
  • Ability to effectively review a statistical analysis plan and to identify deficiencies, errors, and inconsistencies in statistical output
  • Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner.
  • Significant experience as a lead writer in preparing CSRs and protocols, with consistently positive feedback from customers and colleagues.
  • In depth knowledge of drug development, medical writing, and associated regulations. Good understanding of statistical principles and of medical terminology across a range of therapeutic areas.
  • Excellent written and oral communication skills including grammatical/technical writing skills.
  • Excellent attention to detail and accuracy.
  • Confident and effective communication and negotiation skills with customers and project managers.
  • Able to deliver difficult messages in constructive manner.
  • Demonstrates initiative and sound judgement when faced with less familiar project/document situations or challenges.
  • Demonstrated abilities in collaboration with others and independent thought.
  • Demonstrates confidence and maturity in most routine medical writing situations.
  • Demonstrates good judgement in requesting input from senior staff.
  • Ability to establish and maintain effective working relationships with coworkers, managers and customers.
  • Ability to effectively manage multiple tasks and projects.
  • Ability to proactively evaluate risks and potential issues and seek solutions and discuss appropriately with colleagues and customers.
  • Must be computer literate.

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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