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Remote Medical Writer Jobs in Washington (NOW HIRING)

Remote Summary Overview : The Office of Integrated Food Safety System Partnerships (OIFSSP) leads ... The technical writer will develop, revise, and maintain documentation for operational and ...

Technical Writer

Falls Church, VA · On-site +1

$108K - $125K/yr

Goldbelt Apex is seeking a skilled Technical Writer to produce clear, accurate, and compliant ... As an employee, you'll enjoy a comprehensive benefits package, including medical, dental, and ...

Technical Writer

Falls Church, VA · On-site +1

$108K - $125K/yr

As an employee, you'll enjoy a comprehensive benefits package, including medical, dental, and ... Exceptional writing and editing skills, with strong attention to grammar, clarity, structure, and ...

Technical Writer

Falls Church, VA · On-site +1

$108K - $125K/yr

Goldbelt Apex is seeking a skilled Technical Writer to produce clear, accurate, and compliant ... As an employee, you'll enjoy a comprehensive benefits package, including medical, dental, and ...

Kaiva Tech, LLC is seeking part-time Technical Writer.Clearance: Ability to obtain a Public ... remote collaboration and timely completion of assignments. · Must have the ability to send and ...

Technical Writer (0045)

Arlington, VA · Remote

$70K - $100K/yr

Technical Writer (0045) OCT Consulting is a business management and technology consulting firm that ... Medical, Dental, and Vision insurance * Retirement savings 401K plan provided by an industry ...

Technical Writer (0045)

Arlington, VA · On-site +1

$70K - $100K/yr

Technical Writer (0045) OCT Consulting is a business management and technology consulting firm that ... Medical, Dental, and Vision insurance * Retirement savings 401K plan provided by an industry ...

Showing results 21-40

Remote Medical Writer information

See Washington salary details

$16

$43

$65

How much do remote medical writer jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for remote medical writer in Washington is $43.76, according to ZipRecruiter salary data. Most workers in this role earn between $29.66 and $55.29 per hour, depending on experience, location, and employer.

What is a remote medical writer?

Remote medical writers are professionals who create scientific documents, such as clinical study reports, regulatory submissions, medical articles, and educational materials, while working from a location outside of a traditional office setting. They typically have expertise in medical science and strong writing skills, enabling them to communicate complex medical information clearly and accurately. Remote medical writers often collaborate with healthcare professionals, researchers, and pharmaceutical companies using digital tools. Their work is crucial for ensuring that medical content is accurate, compliant with regulations, and accessible to its target audience. This role allows for location flexibility and is increasingly in demand within the healthcare and pharmaceutical industries.

What does a remote medical writer do?

As a remote medical writer, your duties are to work from home and write documents or articles for medical journals, promotional materials, and reports. In this position, you may collect medical information from clinical studies, examine the protocols used in those studies, and edit documents to ensure the clarity and consistency of the content. Most medical writers specialize in a particular type of content, such as writing research proposals or filling out paperwork for regulatory submissions. Although this is a remote position, companies tend to prefer applicants who are located in the same part of the country to make it easier to coordinate schedules and answer questions as needed.

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

To thrive as a Remote Medical Writer, you need strong scientific knowledge, excellent writing skills, and a relevant degree in life sciences or medicine. Familiarity with referencing software, document management systems, and guidelines like ICMJE or AMA is typically required, along with experience using tools such as EndNote or PubMed. Attention to detail, time management, and the ability to communicate complex information clearly are standout soft skills for this role. These abilities are essential for producing accurate, credible, and timely medical content that meets regulatory and publication standards.

How do remote medical writers typically collaborate with subject matter experts and project teams while working offsite?

Remote Medical Writers often work closely with physicians, researchers, and regulatory professionals through virtual meetings, emails, and collaborative document platforms. Regular communication is essential to clarify scientific content, gather feedback, and ensure accuracy in documentation. Tools like Microsoft Teams, Zoom, and cloud-based editing platforms facilitate real-time collaboration and version control. Building strong working relationships and maintaining proactive communication are key to overcoming the challenges of remote teamwork in this role.

What is the difference between Remote Medical Writer vs Medical Communications Specialist?

AspectRemote Medical WriterMedical Communications Specialist
Required CredentialsTypically requires a degree in life sciences, healthcare, or related field; often a medical or scientific writing certificationSimilar credentials; may also require training in medical communication or marketing
Work EnvironmentPrimarily remote, working independently on scientific documentsOften collaborative, working with teams on strategic communication projects
Employer & Industry UsagePharmaceutical, biotech, and healthcare companies; contract agenciesPharmaceutical companies, medical education agencies, and healthcare marketing firms
Common Search & Comparison IntentYesYes

Remote Medical Writers focus on creating scientific documents independently, often remotely, while Medical Communications Specialists typically work in teams to develop broader communication strategies. Both roles require similar scientific backgrounds and are prevalent in healthcare industries, but their daily tasks and collaboration levels differ.

Is there a demand for remote medical writers?

Remote medical writers are in high demand due to the growth of the healthcare and pharmaceutical industries, as well as the increasing need for clear scientific communication. Many companies and organizations seek skilled writers with expertise in medical terminology, regulatory writing, and familiarity with tools like reference management software, making remote opportunities widely available.

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

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

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

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

What cities in Washington are hiring for Remote Medical Writer jobs?

Cities in Washington with the most Remote Medical Writer job openings:

Infographic showing various Remote Medical Writer 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 $91,020 per year, or $43.8 per hour.

Technical Writer

Kaiva Tech

Washington, DC • On-site, Remote

Part-time

Posted 27 days ago


Job description

Kaiva Tech, LLC is seeking part-time Technical Writer.

Clearance: Ability to obtain a Public Trust

Workplace: Remote

Summary Overview:

The Office of Integrated Food Safety System Partnerships (OIFSSP) leads the Human Foods Program's activities to strengthen an integrated food safety system including the implementation of seamless partnerships and operations among federal, state, local, territorial, tribal and international agencies. OIFSSP is directly accountable to the FDA Deputy Commissioner for Human Foods and is responsible for integrating the efforts of all food-related programs across the Agency and for optimizing the use of available resources and methods to enhance the safety, nutritional quality, and labeling of the nation's food supply. Additionally, the office fulfills a critical role in the planning and implementation of recommendations stemming from the Department of Health and Human Services (HHS) Secretary's Making America Healthy Again (MAHA) initiatives. Through these efforts, OIFSSP ensures productive collaboration with both internal and external stakeholders, providing the support necessary to fully realize the Agency's public health objectives.

The technical writer will develop, revise, and maintain documentation for operational and programmatic requirements to support various program initiatives of OIFSSP, with primary focus on the Better Regulatory Inspections for Dynamic Government Efficiency (BRIDGE) and Time/Temperature Control for Safety (TCS) retail food program.

Leveraging strong written and verbal communication skills, the technical writer will support: 1) documentation, including briefing materials, guidance documents, training materials, technical reports, standard operating procedures, and educational resources; 2) stakeholder communication, including Materials that communicate technical and regulatory information to various audiences including regulatory partners, industry stakeholders, and other interested parties; and 3) other written materials defined during the engagement.

Supervisory Responsibilities:

· None.

Essential Duties and Responsibilities:

· Edit, review, and proofread regulatory, technical, policy, procedural, and administrative documents for accuracy, clarity, consistency, grammar, and compliance with organizational standards.

· Ensure documents conform to applicable federal regulations, agency directives, legal requirements, and established editorial style guides.

· Verify consistency of terminology, formatting, citations, references, numbering, and document structure across complex documentation sets.

· Collaborate with subject matter experts (SMEs), program managers, and technical staff to clarify technical content and regulatory requirements.

· Translate complex technical and regulatory information into clear, concise, and audience-appropriate language without altering technical accuracy or legal intent.

· Review documents for completeness, logical organization, readability, and alignment with intended purpose and audience.

· Maintain document quality throughout the review, revision, approval, and publication lifecycle.

· Apply version control and document management practices to ensure traceability, configuration control, and accurate revision histories.

· Manage multiple editing assignments simultaneously while meeting project deadlines.

· Ensure document compliance with accessibility and security requirements.

· Support document review cycles by incorporating stakeholder comments, reconciling conflicting feedback, and documenting editorial decisions.

· Conduct quality assurance reviews to identify inconsistencies, omissions, formatting errors, and compliance risks before publication.

· Develop, maintain, and update document templates, style guides, editorial standards, and writing best practices.

· Ensure consistency across related documents, including regulations, guidance documents, standard operating procedures (SOPs), manuals, reports, and technical specifications.

· Coordinate document routing, approvals, and publication activities using established workflows and document management systems.

· Verify the accuracy of cross-references, hyperlinks, appendices, figures, tables, and citations.

· Edit documents to ensure compliance with plain language principles while preserving technical integrity.

· Maintain confidentiality and appropriately handle sensitive, controlled, or proprietary information.

· Assist authors in interpreting editorial standards, formatting requirements, and document preparation procedures.

· Ensure published documents meet organizational branding, formatting, accessibility, and publication requirements.

· Perform additional technical writing, editing, and documentation support duties as assigned.

Required Experience and Skills:

· Minimum of three (3) years of progressively responsible experience as a Technical Writer, Technical Editor, Regulatory Writer, or Documentation Specialist.

· Experience editing and maintaining complex technical, regulatory, policy, procedural, or administrative documentation in a highly regulated government, defense, healthcare, energy, financial services, or similarly regulated environment.

· Demonstrated experience reviewing documents for compliance with organizational standards, regulatory requirements, and established style guides.

· Experience collaborating with subject matter experts (SMEs), program managers, and cross-functional teams to develop and refine technical documentation.

· Experience managing multiple document review cycles, incorporating stakeholder feedback, and meeting competing deadlines.

· Experience using document management systems, version control processes, and collaborative editing tools.

· Experience supporting document lifecycle management, including drafting, review, and approval.

· Experience maintaining document consistency across large documentation sets, including regulations, policies, procedures, manuals, guidance documents, and reports.

· Experience applying plain language principles while preserving technical accuracy and intent.

· Experience working with Microsoft Office Suite, particularly Microsoft Word's advanced editing, formatting, and document comparison features.

Required Equipment and Work Environment

Contractor is responsible for providing all equipment, software licenses, internet service, and other resources necessary to perform the work, unless otherwise provided by the client.

· Must provide and maintain a reliable personal laptop or desktop computer capable of supporting the duties of the position.

· Must have a licensed version of Microsoft Office (including Microsoft Word, Excel, Outlook, and PowerPoint).

· Must have reliable high-speed internet access to support remote collaboration and timely completion of assignments.

· Must have the ability to send and receive email, participate in virtual meetings, and communicate effectively with Program Managers, technical staff, subject matter experts, and other project stakeholders.

· Must be proficient in using common collaboration and communication platforms (e.g., Microsoft Outlook, Microsoft Teams, SharePoint, or other client-approved tools, as applicable).

· Must maintain a professional remote work environment that supports confidentiality and the secure handling of sensitive or controlled information.

The above statements are intended to describe the general nature and level of work being performed by the individual(s) assigned to this position. They are not intended to be an exhaustive list of all duties, responsibilities, and skills required. Kaiva Corporation reserves the right to modify, add, or remove duties and to assign other duties as necessary. In addition, where applicable and available, reasonable accommodation(s) may be made to enable individuals with disabilities to perform essential functions of this position. Kaiva Corporation is a proud Equal Opportunity Employer! All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability or veteran status