ZipRecruiter

Log In

1

Medical Writing Jobs in Washington (NOW HIRING)

KME Digital

Content Writing Intern

Alexandria, VA · On-site

As a KME.digital Content Writing Intern, you will write and edit marketing content, particularly blogs and website copy, for numerous businesses. You will also collaborate with our close-knit team to ...

Labcorp

Senior Medical Courier

Chantilly, VA · On-site

$17.75 - $26/hr

Labcorp is seeking a Medical Courier II to join our team in Chantilly, VA. Work Schedule: Monday - Friday 12:00pm - 3:00am; (must be flexible) Job Responsibilities: * Act as a floater for the ...

Otsuka

Director, Global Clinical Development

Rockville, MD · On-site +1

$209K - $313K/yr

Working knowledge of associated disciplines, including immunology, biostatistics, clinical pharmacology, formulation science, data management, and medical writing. * Complete understanding of the ...

previous pagenext page

Showing results 21-40

All JobsMedical Writing JobsMedical Writing Jobs in Washington

Medical Writing information

See Washington salary details

$13

$52

$89

How much do medical writing jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for medical writing in Washington is $52.40, according to ZipRecruiter salary data. Most workers in this role earn between $38.12 and $63.41 per hour, depending on experience, location, and employer.

What is medical writing?

Medical writing is the process of creating scientific documents by specialized writers in the healthcare, pharmaceutical, or biotechnology industries. These documents can include clinical trial reports, regulatory submissions, research manuscripts, patient education materials, and more. Medical writers must accurately present complex medical information in a clear, concise, and compliant manner, often working closely with researchers, doctors, and regulatory professionals. The role requires a strong understanding of medical terminology, scientific research, and regulatory guidelines.

What are medical writing jobs?

Medical writing jobs work in health care and science communities to compose documents and articles. Those who have medical writing jobs may draft many different kinds of papers, such as educational or promotional literature, medical abstracts for textbooks, or research documents. Other medical writing jobs include ghost-writing for prominent scientists or physicians, journalistic writing for scientific magazines, or creating content for marketing materials. Regardless of what field you are in, to obtain medical writing jobs, you must be able to decipher and interpret complicated information and write in a manner that your audience understands. For example, you may use medical jargon in scientific journals, but medical writers typically use simpler language when writing for the general public.

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 strong scientific knowledge, excellent written communication skills, and typically a background in life sciences or healthcare. Familiarity with referencing software, regulatory guidelines, and document management systems is often required. Attention to detail, adaptability, and the ability to explain complex concepts clearly are valuable soft skills in this role. These abilities ensure the accurate and effective communication of medical information for regulatory, clinical, or educational purposes.

How does a medical writer typically collaborate with subject matter experts and regulatory teams during a project?

Medical writers regularly interact with subject matter experts (such as clinicians and researchers) to ensure scientific accuracy and clarity in documents like clinical study reports, publications, or regulatory submissions. They also work closely with regulatory teams to align content with current guidelines and submission requirements. This collaboration often involves attending meetings, managing document reviews, and incorporating diverse feedback to produce high-quality, compliant deliverables. Effective communication and project management skills are essential to coordinate these multi-disciplinary efforts and meet strict deadlines.

What is the difference between Medical Writing vs Medical Editing?

AspectMedical WritingMedical Editing
Required CredentialsTypically requires a background in life sciences, healthcare, or related fields; often a degree or certification in medical writingRequires strong knowledge of medical terminology and writing; often a background in healthcare, editing, or related fields
Work EnvironmentOften works independently or in teams, creating clinical documents, regulatory submissions, and educational materialsUsually works alongside writers, reviewing and refining medical documents for clarity, accuracy, and consistency
Employer & Industry UsageUsed in pharmaceutical, biotech, healthcare, and medical device industriesCommon in publishing, healthcare communications, and regulatory agencies

Medical Writing involves creating original medical content such as clinical study reports, regulatory documents, and educational materials. Medical Editing focuses on reviewing and refining these documents to ensure clarity, accuracy, and compliance. Both roles require strong medical knowledge, but Medical Writers produce content, while Medical Editors improve existing content.

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 or those with specialized skills can earn over $100,000 per year. Many medical writers also have opportunities for freelance work or consulting, which can impact income levels.

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 complemented by advanced degrees or certifications in medical writing or regulatory writing. Developing strong writing skills, understanding scientific and medical terminology, and gaining experience through internships or entry-level positions are important steps; familiarity with tools like Microsoft Word and reference management software can also be beneficial.

Is there a demand for medical writers?

Yes, there is a strong demand for medical writers due to the growth of the healthcare and pharmaceutical industries, regulatory requirements, and the need for clear scientific communication. Medical writers often work in pharmaceutical companies, medical communications agencies, or as freelancers, and proficiency in scientific terminology and regulatory guidelines enhances job prospects.

What does the medical writer do?

A medical writer creates clear, accurate, and scientifically supported documents such as research articles, regulatory submissions, clinical study reports, and patient education materials. They interpret complex medical data for diverse audiences and often work with subject matter experts, adhering to industry guidelines and using tools like reference management software. Strong writing skills and knowledge of medical terminology are essential for this role.
More about Medical Writing jobs

What are the most commonly searched types of Medical Writing jobs in Washington?

The most popular types of Medical Writing jobs in Washington are:

What are popular job titles related to Medical Writing jobs in Washington?

For Medical Writing jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Medical Writing jobs in Washington look for?

The top searched job categories for Medical Writing jobs in Washington are:

What cities in Washington are hiring for Medical Writing jobs?

Cities in Washington with the most Medical Writing job openings:

Medical Writing jobs near you
Infographic showing various Medical Writing job openings in Washington as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 12% Part Time, 2% Temporary, and 10% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $108,996 per year, or $52.4 per hour.

Director, Scientific Writing

AstraZeneca GmbH

Gaithersburg, MD • On-site

$164.98 - $210.65/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 18 days ago

Job description

Introduction to Role:

Do you have expertise in and passion for Medical Affairs in Oncology? AstraZeneca’s vision in Oncology is to help patients by redefining the cancer‑treatment paradigm with the bold ambition to eliminate cancer as a cause of death. We are proud to work on groundbreaking science with one of the broadest and deepest Oncology pipelines in the business! Help to advance our pipeline by applying expertise and accelerating our pathway to finding a cure.

The Centre of Oncology Data Excellence (CODE) is a team within Global Medical Evidence Generation organization that is passionate about delivering outstanding class scientifically rigorous research to support the Global and US Medical Affairs (GMA). Director, Scientific Writing reports to the Head, CODE and will be leading and running a high‑performing scientific writing function, overseeing a blended team of internal writers and contractors to deliver high‑quality outputs across interventional trials and real‑world/observational studies. The Director will be a champion of AI‑augmented writing workflows and responsible for building the capability and culture to embrace these tools responsibly and effectively.

Responsibilities

  • Lead the development of protocols, and study reports for global and US Oncology medical affairs clinical interventional studies from Phase II–IV.

  • Personally author and provide oversight of scientific writing outputs (abstracts, posters, manuscripts, study reports, protocols, HTA dossier summaries) for real‑world evidence and observational studies conducted by the Oncology Outcomes Research team, including database studies, registry analyses, and chart reviews.

  • Lead the AI adoption roadmap for scientific writing: evaluate, pilot, and scale AI‑assisted drafting, literature synthesis, and quality review tools; establish governance frameworks for responsible use; train and upskill the team; and track measurable impact on quality, speed, and capacity.

  • Lead budgets, contractor relationships, and performance of internal and external scientific writers.

  • Collaborate with Oncology Outcomes Research and Evidence Delivery Team (delivering interventional trials) regarding the planning and development of scientific writing deliverables.

  • Represent Scientific Writing team as a member of CODE Leadership team.

Essential Qualifications

  • Advanced degree in a scientific or medical field (e.g., PharmD, PhD, MD).

  • At least 7 years experience in scientific writing.

  • Demonstrated experience in the publications field, or medical communications gained through working in the pharmaceutical industry or a medical communications agency.

  • Broad understanding of drug development process.

  • Hands‑on proficiency with AI writing tools (e.g., Claude, Copilot, Gemini) and demonstrated ability to critically evaluate outputs for scientific accuracy, regulatory alignment, and compliance with GPP/ICMJE standards; understanding of where AI can and cannot be applied in regulated medical writing contexts.

  • Demonstrated performance, budget, and resource management skills in a global organization.

  • Be independent, organized, and able to act as a leader in a fast‑paced environment.

  • Ensure strict adherence to company policies, industry regulations, and ethical standards in all publications.

  • Flexibility and adaptability to lead long‑term activities in a constantly changing internal and external environment.

Desirable

  • Therapeutic knowledge in oncology.

  • Knowledge of publication management systems.

  • Certification as a Medical Publication Professional (CMPP) desired.

  • Validated experience crafting and scaling AI‑enabled workflows (e.g., timelylibraries, automated literature review, structured output templates), with measurable impact on timelines, throughput, or quality; comfort operating in a regulatory environment where AI use must be disclosed, validated, and defensible.

The annual base pay for this position ranges from $164,981 to $210,651. Hourly and salaried non‑exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job‑related knowledge, skills, and experience. In addition, our positions offer a short‑term incentive bonus opportunity; eligibility to participate in our equity‑based long‑term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered include a qualified retirement program (401(k) plan); paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at‑will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

#J-18808-Ljbffr

Apply