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Remote Scientific Technical Writer Jobs (NOW HIRING)

OCT Consulting, LLC

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 ... Role: • Draft and revise scientific/technical documentation in simple languages to be understood ...

OCT Consulting, LLC

Technical Writer (0045)

Arlington, VA · Remote

$70K - $100K/yr

Technical Writer (0045) OCT Consulting is a business management and technology consulting firm that ... Role: ● Draft and revise scientific/technical documentation in simple languages to be understood ...

H R Computer Consulting Services

NEPA-ESA Writer

$100K - $110K/yr

Remote (Off-site) Employment Type: Full-Time Contractor Position Overview NOAA National Marine ... Review and edit scientific documents for technical accuracy, clarity, consistency, organization ...

ERP International

Technical Writer

Fort George G Meade, MD · On-site +1

$70K - $85K/yr

Primarily remote, however, may be required to be at customer site at Fort Meade on occasion. Must ... health, science, and technology solutions supporting clients in the government and commercial ...

Noblesoft Technologies

Technical Writer

Secaucus, NJ · Remote

Job Role - Technical Writer Location - Secaucus, NJ(Remote) Qualifications: Education Preferred: Bachelor's degree in Technical Writing, Communication or equivalent. Work Experience: 3+ years of ...

Lorven Technologies

Technical Writer

Primarily remote work with some planned onsite work in Jackson, MS Remote with occasional travel onsite Rate: xxx/hr on C2C All Inclusive or xxx/hr on W2 Without Benefits State Agency: MS MDCPS ...

Jobgether

$127K - $190K/yr

As a Technical Writer, you will join a global, remote-first environment where you will shape how developers and technical users interact with complex software solutions. You will own documentation ...

Changeis

Technical Writer

Most of our positions are remote, offering flexibility while working on impactful projects. Key Skills amp; Qualifications We're Looking For: * Technical Writing: Proven experience in creating clear ...

InstantServe LLC

Technical Writer

Remote Position Overview The State Court Administrator's Office (Court Services Division) is seeking a Technical Writer/Data Specialist for a short-term, one-month project . Important: This ...

DivIHN

Technical Writer V (Remote)

Technical Writer V (Remote) Duration: 5 Months Location: Remote Only W2 candidates are eligible for this position. Third-party or C2C candidates will not be considered. Role is open to remote ...

Spatial Front, Inc.

Technical Writer

$50K - $75K/yr

... is seeking a Technical Writer to support our federal software development program. The ideal ... This is a remote, full-time, W2 role. Key Responsibilities: * Develop, edit, and maintain end-user ...

Lorven Technologies

Technical Writer

Denver, CO · On-site +1

Job Title: Technical Writer Location: Denver, CO - Remote Duration: 1 Months Contract QUALIFICATIONS: Microsoft Excel 2010/2013 Duties and Responsibilities: This person would be transcribing past ...

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How much do remote scientific technical writer jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for remote scientific technical writer 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 a remote scientific technical writer?

A Remote Scientific Technical Writer is a professional who creates clear and accurate documentation related to scientific topics, such as research papers, instruction manuals, protocols, or technical reports, while working from a location outside of a traditional office. They often collaborate with scientists, engineers, and subject matter experts to translate complex scientific information into understandable content for various audiences. Their work is essential in ensuring scientific concepts and research findings are communicated effectively and meet regulatory or publication standards. Working remotely allows them to perform these tasks from anywhere with a reliable internet connection.

What are the key skills and qualifications needed to thrive as a remote scientific technical writer?

To thrive as a Remote Scientific Technical Writer, you need a strong background in science or engineering, excellent writing skills, and typically a degree in a relevant field. Familiarity with style guides, reference management software, and document collaboration tools like Microsoft Word and Google Docs is important. Exceptional attention to detail, self-motivation, and the ability to communicate complex information clearly are critical soft skills. These abilities ensure accurate, accessible documentation that supports scientific communication and collaboration in a remote setting.

What is the difference between Remote Scientific Technical Writer vs Remote Scientific Content Developer?

AspectRemote Scientific Technical WriterRemote Scientific Content Developer
CredentialsBachelor's or higher in science/engineering, technical writing certificationsSimilar credentials, often with additional focus on content creation skills
Work EnvironmentRemote, collaborating with scientists and engineersRemote, creating educational or marketing scientific content
Industry UsageUsed in biotech, pharma, research institutionsCommon in science education, marketing, and corporate communications
Search/Comparison IntentUnderstanding technical writing roles in scienceExploring content creation roles in scientific fields

The Remote Scientific Technical Writer and Remote Scientific Content Developer roles share similar credentials and work environments, often within biotech, pharma, or research sectors. While technical writers focus on creating clear, precise documentation, content developers emphasize engaging scientific content for education or marketing. Both roles require scientific knowledge and strong writing skills, but their end goals and content types differ slightly.

How does a remote scientific technical writer typically collaborate with subject matter experts and team members given the remote work setup?

As a Remote Scientific Technical Writer, collaboration with subject matter experts (SMEs) and team members is primarily facilitated through digital communication tools such as email, video conferencing, and project management platforms. Regular virtual meetings and clear documentation processes are essential to clarify technical concepts and ensure accuracy. Writers often coordinate with researchers, scientists, and editors across different time zones, requiring strong organizational skills and proactive communication. Building rapport remotely and maintaining open lines of feedback are key to producing high-quality, precise scientific documentation.
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What cities are hiring for Remote Scientific Technical Writer jobs? Cities with the most Remote Scientific Technical Writer job openings:
What are the most commonly searched types of Scientific Technical Writer jobs? The most popular types of Scientific Technical Writer jobs are:
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Remote Scientific Technical Writer jobs near you
Infographic showing various Remote Scientific Technical Writer job openings in the United States as of July 2026, with employment types broken down into 72% Full Time, 8% Part Time, and 20% Contract. Highlights an 42% Physical, 3% Hybrid, and 55% Remote job distribution, with an average salary of $98,010 per year, or $47.1 per hour.

Scientific Technical Writer

Medpace, Inc.

Cincinnati, OH • On-site, Remote

Other

Medical, Retirement, PTO

Re-posted 24 days ago

Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

14th of 72 rated research

Job description

Job Summary

Our bioanalytical services are growing rapidly, and we are currently seeking a full-time, office based Scientfic Technical Writer to join our team. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities
  • Assist Scientists to prepare protocols, methods and reports for sponsors' studies;
  • Organize study documents, such as, notebooks, sample receiving documents, CoAs of reference standards, etc., for individual studies;
  • Compile and review all results from instruments and Watson-LIMS database for report writing;
  • Able to use templates to prepare protocols and reports for scientists in an efficient manner.
Qualifications
  • A minimum of a Bachelor's degree, with previous experience in a research laboratory;
  • Writing communication prefered;
  • Knowledge of GLP, cGMP, and ICH guidelines;
  • Strong organizational and communication (written and oral) skills; and
  • Knowledge of Microsoft Word, Excel, and Powerpoint.

Travel: None

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience

    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Employment Type: OTHER

What Medpace employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992

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