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Remote Senior Science Writer Jobs (NOW HIRING)

Ambition 24Hours Inc

Senior Medical Writer

The Lakes, NV · Remote

$142K - $195K/yr

Senior Medical Writer - Full-Time Remote Opportunity ───── Location: Fully Remote (U.S ... This fully remote opportunity is ideal for a highly skilled clinical science writer with extensive ...

Integrated Resources INC

Sr. Medical Writer

Mansfield, MA · On-site +1

... 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 ...

Stryker

Senior Staff Medical Writer (Remote)

Portland, OR · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... As the Senior Staff Medical Writer , you will develop scientific and clinical documentation that ...

Stryker

Senior Staff Medical Writer (Remote)

San Diego, CA · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... As the Senior Staff Medical Writer , you will develop scientific and clinical documentation that ...

Stryker

Senior Staff Medical Writer (Remote)

Denver, CO · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... As the Senior Staff Medical Writer , you will develop scientific and clinical documentation that ...

Stryker

Senior Staff Medical Writer (Remote)

Denver, CO · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... As the Senior Staff Medical Writer , you will develop scientific and clinical documentation that ...

Stryker

Senior Staff Medical Writer (Remote)

Phoenix, AZ · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... As the Senior Staff Medical Writer , you will develop scientific and clinical documentation that ...

Stryker

Senior Staff Medical Writer (Remote)

Seattle, WA · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... As the Senior Staff Medical Writer , you will develop scientific and clinical documentation that ...

Stryker

Senior Staff Medical Writer (Remote)

Los Angeles, CA · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... As the Senior Staff Medical Writer , you will develop scientific and clinical documentation that ...

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Remote Senior Science Writer information

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$30.5K

$92.6K

$171K

How much do remote senior science writer jobs pay per year?

As of Sep 8, 2026, the average yearly pay for remote senior science writer in the United States is $92,559.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,000.00 and $101,000.00 per year, depending on experience, location, and employer.

What does a remote senior science writer do?

A Remote Senior Science Writer is responsible for creating, editing, and reviewing scientific content for a variety of audiences, such as academic journals, research institutions, or the general public, all while working from a remote location. They translate complex scientific concepts into clear, accurate, and engaging materials like articles, reports, white papers, or grant proposals. Senior Science Writers often collaborate with researchers, subject matter experts, and editors to ensure scientific accuracy and accessibility. Their role may also involve mentoring junior writers, managing projects, and staying updated on the latest developments in science and science communication.

What are some common challenges faced by remote senior science writers when collaborating with global research teams?

Remote Senior Science Writers often work with international research teams, which can present challenges such as navigating time zone differences, ensuring clear communication despite cultural and language barriers, and managing multiple collaborative platforms. To succeed, writers need to be proactive in scheduling meetings, use collaborative tools effectively, and maintain organized documentation of revisions and feedback. Building strong relationships with team members and setting clear expectations for project timelines can help streamline the writing and review process.

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

To thrive as a Remote Senior Science Writer, you need advanced writing and editing skills, a strong background in science (often at least a bachelor’s or master’s degree), and experience translating complex scientific concepts for diverse audiences. Familiarity with reference management software, content management systems (CMS), and proficiency with collaborative tools like Google Workspace are typically required. Outstanding attention to detail, time management, and the ability to communicate clearly with both subject-matter experts and non-experts are crucial soft skills. These competencies ensure clear, accurate, and engaging science communication that meets publication standards and client needs in a remote work environment.
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Remote Senior Science Writer jobs near you
Infographic showing various Remote Senior Science Writer job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 77% Full Time, 19% Part Time, and 2% Contract. Highlights an 75% Physical, 3% Hybrid, and 22% Remote job distribution, with an average salary of $92,559 per year, or $44.5 per hour.

Senior Medical Writer

Ambition 24Hours Inc

The Lakes, NV • Remote

$142K - $195K/yr

Contractor

Re-posted 18 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
───────────────────────────

Job Overview
───────────────────────────
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.

───────────────────────────
Key Responsibilities
───────────────────────────
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

───────────────────────────
Requirements
───────────────────────────
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

───────────────────────────
Ideal Candidate Profile
───────────────────────────
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