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Remote Development Writer Jobs (NOW HIRING)

Senior Medical Writer

The Lakes, NV · Remote

$142K - $195K/yr

... development and regulatory documentation activities within a leading biotechnology environment. This fully remote opportunity is ideal for a highly skilled clinical science writer with extensive ...

Primarily remote work with some planned onsite work in Jackson, MS Remote with occasional travel ... State of Mississippi The Technical Writer will support the planning, development, implementation ...

Grant Writer

New York, NY · On-site +1

$5.3K/mo

Contributing to the development, maintenance, and expansion of core grant writing resources ... Experience working in remote contexts, with globally distributed team members, and demonstrating ...

Theseniormedical writer will partner cross-functionallywith client teams inClinical Development ... development underbrisktimelines. Location: Fully remote, but must be able to attend key (e.g ...

Remote and hybrid working options as standard * Continuous learning and professional development ... Job code: CPT407 Career opportunities Medical writing Role Publications Locations USA (Remote ...

Systems Support Engineer

Tacoma, WA · On-site +1

$55 - $58/hr

Initially, focus on helping customers resolve issues connecting to remote development environments ... written interaction with engineers, alongside excellent ticket hygiene (status updates, severity ...

The Front Row SEO & Content team is expanding our network of remote freelance Content Writers to ... Paid Professional Development Opportunities * A fast-paced, high energy & dog friendly office space ...

Theseniormedical writer will partner cross-functionallywith client teams inClinical Development ... development underbrisktimelines. Location: Fully remote, but must be able to attend key (e.g ...

... the end-to-end product development process. You will collaborate closely with product and ... The UX Writer will work closely with designers, researchers, product managers, and other ...

... the end-to-end product development process. You will collaborate closely with product and ... The UX Writer will work closely with designers, researchers, product managers, and other ...

... the end-to-end product development process. You will collaborate closely with product and ... The UX Writer will work closely with designers, researchers, product managers, and other ...

... the end-to-end product development process. You will collaborate closely with product and ... The UX Writer will work closely with designers, researchers, product managers, and other ...

... product development. The primary responsibilities of the position are organizing, analyzing ... Benefits vary by location and may include: o Remote working o Flexible time off o Paid holidays o ...

... product development. The primary responsibilities of the position are organizing, analyzing ... Benefits vary by location and may include: o Remote working o Flexible time off o Paid holidays o ...

... product development. The primary responsibilities of the position are organizing, analyzing ... Benefits vary by location and may include: o Remote working o Flexible time off o Paid holidays o ...

... product development. The primary responsibilities of the position are organizing, analyzing ... Benefits vary by location and may include: o Remote working o Flexible time off o Paid holidays o ...

... product development. The primary responsibilities of the position are organizing, analyzing ... Benefits vary by location and may include: o Remote working o Flexible time off o Paid holidays o ...

Showing results 41-60

Remote Development Writer information

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$47K

$67.6K

$88.5K

How much do remote development writer jobs pay per year?

As of Aug 16, 2026, the average yearly pay for remote development writer in the United States is $67,603.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,000.00 and $78,500.00 per year, depending on experience, location, and employer.

What is the difference between Remote Development Writer vs Remote Content Writer?

AspectRemote Development WriterRemote Content Writer
Required CredentialsTechnical writing skills, familiarity with development topics, possibly coding knowledgeStrong writing skills, general research ability, SEO knowledge
Work EnvironmentTypically collaborates with developers, tech teams, and product managersWorks with marketing teams, editors, and content strategists
Employer & Industry UsageTech companies, software firms, development agenciesMedia outlets, marketing agencies, corporate blogs
Search & Comparison IntentUnderstanding technical writing roles in developmentExploring general content creation roles

Remote Development Writers focus on creating technical documentation, tutorials, and guides related to software development, requiring technical expertise. Remote Content Writers produce a broader range of content, including blogs, articles, and marketing materials, with less technical specialization. Both roles are remote, but their target industries and skill sets differ significantly.

What cities are hiring for Remote Development Writer jobs?

Cities with the most Remote Development Writer job openings:

What are the most commonly searched types of Development Writer jobs?

The most popular types of Development Writer jobs are:

What states have the most Remote Development Writer jobs?

States with the most job openings for Remote Development Writer jobs include:

Senior Medical Writer

Ambition 24Hours Inc

The Lakes, NV • Remote

$142K - $195K/yr

Contractor

Re-posted 25 days ago


Job description

Senior Medical Writer – Full-Time Remote Opportunity

───────────────────────────
Location: Fully Remote (U.S.)
Industry: Pharmaceutical / Biotechnology
Employment Type: Full-Time
Salary Range: $142,100 – $195,360 annually
Experience Level: Mid-Senior
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Job Overview
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We are seeking an experienced Senior Medical Writer to support clinical development and regulatory documentation activities within a leading biotechnology environment. This fully remote opportunity is ideal for a highly skilled clinical science writer with extensive experience authoring Clinical Study Reports (CSRs), protocols, and regulatory submission documents across Phase I–III studies.

The ideal candidate is a hands-on writer who spends the majority of their time authoring and developing scientific and regulatory documents rather than primarily editing or managing teams. Strong expertise in clinical development, regulatory writing standards, and cross-functional collaboration is essential.

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Key Responsibilities
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Author and edit clinical study documents including protocols, protocol amendments, informed consent forms, and Clinical Study Reports (CSRs)
Prepare regulatory submission documents including briefing books and eCTD summaries/modules
Draft aggregate safety and efficacy documents including DSURs, PBRERs, and Investigator Brochures
Manage document timelines, review cycles, and comment adjudication processes
Lead and facilitate document-related meetings with cross-functional study teams
Collaborate with clinical, biostatistics, regulatory, pharmacovigilance, and data management teams
Interpret and present complex clinical data in clear scientific narratives, tables, and graphics
Ensure all documentation complies with regulatory guidelines, industry standards, and internal style guides
Support process improvements, templates, and standard operating procedures within Medical Writing

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Requirements
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Bachelor’s degree or higher in a scientific discipline required
7–10+ years of medical writing experience within biotech, pharmaceutical, or CRO environments
Extensive experience authoring Clinical Study Reports (CSRs) and protocol amendments required
Experience with INDs, NDAs, BLAs, DSURs, PBRERs, and regulatory briefing books strongly preferred
Strong understanding of clinical development processes and regulatory requirements
Experience with eCTD submissions and Modules 2–5 preferred
Ability to interpret complex clinical and statistical data
Excellent scientific writing, communication, and organizational skills
Proficiency with Microsoft Office Suite, Adobe Acrobat, Veeva, SharePoint, or similar document management systems
Ability to manage multiple projects and work independently in a remote environment

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Ideal Candidate Profile
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Highly experienced clinical medical writer with strong Phase I–III study expertise
Focused primarily on authoring scientific and regulatory content rather than editing or project management
Demonstrated excellence in CSR development and clinical science documentation
Biotech or pharmaceutical industry background strongly preferred
CRO experience considered
Strong attention to detail with the ability to meet strict timelines and regulatory standards