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Commission Principal Medical Writer Jobs in Raleigh, NC

Principal Medical Writer

Durham, NC · On-site

$90 - $120/hr

Principal Medical Writer ViiV Healthcare, a global specialty HIV company, is seeking a Principal Medical Writer who will lead and deliver high-quality medical writing for complex clinical and ...

Overview We are seeking an experienced Principal Medical Writer to lead the development of high-quality clinical and regulatory documents supporting global regulatory submissions. This role plays a ...

Overview We are seeking an experienced Principal Medical Writer to lead the development of high-quality clinical and regulatory documents supporting global regulatory submissions. This role plays a ...

Overview We are seeking an experienced Principal Medical Writer to lead the development of high-quality clinical and regulatory documents supporting global regulatory submissions. This role plays a ...

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 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 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 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 ...

Principal Medical Writier

Durham, NC · On-site

$84 - $211/hr

Principal****Medical 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 ...

... writing queries, joins, views, etc) * Knowledge of software testing practices (test-driven ... medical, dental, and vision plans, life insurance, disability insurance, wellness programs ...

Well-developed written and verbal communication skills including presentations, chairing meetings ... innovative medical treatments to help improve patient outcomes and population health worldwide.

Senior Principal Engineer

Raleigh, NC · On-site

$90 - $120/hr

Position requires a positive attitude along with excellent written communication and interpersonal ... family medical, dental and vision insurance, paid time off, holidays, short-term and long-term ...

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Commission Principal Medical Writer information

See Raleigh, NC salary details

$10.7K

$181.3K

How much do commission principal medical writer jobs pay per year?

As of Aug 27, 2026, the average yearly pay for commission principal medical writer in Raleigh, NC is $180,184.00, according to ZipRecruiter salary data. Most workers in this role earn between $179,800.00 and $180,300.00 per year, depending on experience, location, and employer.

What is the difference between Commission Principal Medical Writer vs Medical Writer?

AspectCommission Principal Medical WriterMedical Writer
CredentialsTypically requires advanced degrees (MD, PhD) and experience in clinical writingUsually holds a bachelor's or master's degree in life sciences or related fields
Work EnvironmentWorks in pharmaceutical or biotech companies, often leading teamsWorks in similar settings, often under supervision or as part of a team
Industry UsageCommonly employed in clinical development, regulatory submissions, and medical communicationsUsed across medical communications, publications, and regulatory documents

The Commission Principal Medical Writer typically has more experience, advanced credentials, and leadership responsibilities compared to a Medical Writer. While both roles focus on medical writing, the Principal often oversees projects and manages teams, whereas the Medical Writer primarily produces content under guidance.

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

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

Infographic showing various Commission Principal Medical Writer job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 12% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $180,184 per year, or $86.6 per hour.

Principal Medical Writer

Durham, NC • On-site

$90 - $120/hr

Other

Re-posted 17 days ago


Job description

Principal Medical Writer

ViiV Healthcare, a global specialty HIV company, 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, regulatory, statistical, and cross‑functional teams. This role offers visible impact, professional growth, and meaningful work that aligns with GSK’s mission of uniting science, technology and talent to get ahead of disease together.

We value scientific rigor, clear communication, collaboration, and ownership.

Responsibilities
  • 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 projects, coordinating contributors, timelines, and quality checks to meet regulatory and internal standards.
  • Translate complex clinical and statistical data into clear, accurate, and well‑structured scientific narratives for diverse audiences.
  • Act as a subject matter expert on medical writing standards, document structure, and regulatory expectations.
  • Drive process improvement initiatives, support KPI tracking, and contribute to audit readiness and compliance activities.
Basic Qualifications
  • Bachelor’s degree in life sciences, health sciences, or a scientific field.
  • 5+ years of experience in medical or regulatory writing within the pharmaceutical or healthcare industry.
  • 3+ years of experience with regulatory dossier development and Common Technical Document (CTD) module documents.
  • 3+ years of experience independently authoring clinical protocols, clinical study reports, and regulatory submission documents.
Preferred Qualifications
  • Advanced degree (e.g., PhD, PharmD, MPH, MS) in life sciences or a related field.
  • Experience leading regulatory submission projects, including Common Technical Document (CTD) dossiers.
  • Familiarity with statistical concepts and ability to interpret clinical data.
  • Strong problem‑solving skills and ability to adapt to changing priorities.
  • Experience working in multicultural or remote team settings.
  • Proven ability to independently write and manage complex regulatory documents.
  • Strong understanding of International Council for Harmonization (ICH) guidelines and Good Clinical Practice (GCP).
  • Excellent written and verbal communication skills, with attention to detail.
  • Experience managing multiple projects and meeting deadlines in a fast‑paced environment.
Benefits

Learn more about the comprehensive benefits program GSK offers US employees. Please visit GSK US Benefits Summary.

Equal Opportunity Employer

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, parental status, national origin, age, disability, genetic information, military service or any basis prohibited under federal, state or local law.

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