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Remote Science Writer Internship Jobs (NOW HIRING)

Senior Medical Writer

The Lakes, NV · Remote

$142K - $195K/yr

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 ...

Remote, US-based WHO WE ARE: MGT is a leading provider of technology and advisory solutions serving ... Experience (professional, internship, or volunteer) in teaching preferred WHAT WE OFFER: Our world ...

$13 - $17.50/hr

If you love using innovative technology to tackle tough science problems and working in a fast ... As an intern, you will learn how to implement novel, cutting-edge remote sensing and machine ...

... Scientific Communications group. Remote candidates are an option. Local candidate to Mansfield, MA preferred. Essential functions: * This role predominantly focuses on writing, editing and reviewing ...

... in scientific and technological subjects. This position needs an individual who can conduct ... Remote work is anticipated. However, all candidates should be local to the Washington, DC metro ...

... in scientific and technological subjects. This position needs an individual who can conduct ... Remote work is anticipated. However, all candidates should be local to the Washington, DC metro ...

Writer/Journalist Internship: The role is focused on content creation for BORGEN Magazine or The Borgen Project Blog. This is a part-time 12-hours per week, 12 week, unpaid remote internship. If your ...

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Remote Science Writer Internship information

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How much do remote science writer internship jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for remote science writer internship in the United States is $47.12, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $58.65 per hour, depending on experience, location, and employer.

What is the difference between Remote Science Writer Internship vs Remote Science Content Coordinator?

AspectRemote Science Writer InternshipRemote Science Content Coordinator
Required CredentialsRelevant science degree or coursework, writing samplesSimilar credentials, often with additional project management skills
Work EnvironmentRemote, internship setting, entry-levelRemote, coordinating content teams, more experienced
Employer & Industry UsageResearch institutions, science media, publishingScientific organizations, media outlets, educational platforms
Search & Comparison IntentEntry-level science writing roles, internshipsContent management, team coordination roles

The Remote Science Writer Internship focuses on developing writing skills in a remote setting for those starting their science communication careers. In contrast, the Remote Science Content Coordinator involves managing and coordinating content creation, requiring more experience. Both roles are remote and industry-specific, but they differ in responsibilities and career level.

What is a Remote Science Writer Internship?

A Remote Science Writer Internship is a position where interns work from home or another remote location to create, edit, and review science-related content. Interns may write articles, summaries, reports, or social media posts about scientific topics, often translating complex research into accessible language for a wider audience. This type of internship offers valuable experience in scientific communication, research, and writing, and is typically suited for students or recent graduates with a background in science and an interest in journalism or science communication.

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

To thrive as a Remote Science Writer Intern, you need strong writing, research, and analytical skills, often supported by a background in science or journalism. Familiarity with citation styles, scientific databases, and content management systems is typically required. Exceptional communication, attention to detail, and time management are crucial soft skills for standing out in this role. These skills ensure accurate, engaging, and timely science communication to a broad audience in a remote work environment.

What are some common challenges faced by remote science writer interns, and how can they be addressed?

Remote science writer interns often face challenges such as managing time effectively across different projects, staying motivated without in-person supervision, and ensuring clear communication with editors and team members. To overcome these, it's helpful to establish a structured daily routine, set clear deadlines, and utilize collaboration tools like Slack or Trello for regular updates. Additionally, proactively seeking feedback and participating in virtual meetings can foster connection and support professional growth.
More about Remote Science Writer Internship jobs
What cities are hiring for Remote Science Writer Internship jobs? Cities with the most Remote Science Writer Internship job openings:
What states have the most Remote Science Writer Internship jobs? States with the most job openings for Remote Science Writer Internship jobs include:
Infographic showing various Remote Science Writer Internship job openings in the United States as of June 2026, with employment types broken down into 12% Internship, 46% Full Time, 26% Part Time, 2% Temporary, and 14% Contract. Highlights an 100% Remote job distribution, with an average salary of $98,010 per year, or $47.1 per hour.

Senior Medical Writer

Ambition 24Hours Inc

The Lakes, NV • Remote

$142K - $195K/yr

Contractor

Posted 22 days ago


Job description

Senior Medical Writer – Full-Time Remote Opportunity

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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