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Remote Scientific Writing Jobs (NOW HIRING)

MedSchoolCoach

Research Mentor

Boston, MA · Remote

$75 - $100/hr

Remote | Part-Time | $75-$100 per session About the Program: The MedSchoolCoach Research Mentorship ... methodology, data collection, scientific writing, and even the publication process.

MedSchoolCoach

Research Mentor

Boston, MA · On-site +1

$75 - $100/hr

... methodology, data collection, scientific writing, and even the publication process ... Remote (Must have stable internet access) ⏳ Part-time, flexible hours

Managed Staffing

Biocompatibility Scientist

FL · Remote

$145 - $150/hr

Remote (Client HQ: Gainesville, FL - No relocation required) Job Summary We are seeking an ... Excellent communication, scientific writing, and project management skills. Preferred ...

Radiance Technologies

The individual will support advanced remote sensing exploitation functions through detailed ... Strong technical writing and briefing skills Desired Skills and Qualifications: * Interpretation of ...

Merican

Medical Writer

Remote Shift: Mon-Fri 9.00 AM-5.00 PM * We are seeking a skilled Medical Writer to develop high ... Excellent scientific writing, editing, and document structuring skills * Ability to simplify ...

YO IT Consulting

Biology QA Lead - Remote

... scientific writing, technical review, quality control, biotechnology, life sciences, or related ... supporting remote teams of trainers, annotators, reviewers, researchers, technical writers ...

YO IT Consulting

Biology QA Lead - Remote

... scientific writing, technical review, quality control, biotechnology, life sciences, or related ... supporting remote teams of trainers, annotators, reviewers, researchers, technical writers ...

Flywheel Partners

Medical Writer

Manhattan, NY · Remote

$65K - $85K/yr

Writing/Content Development * Research, learn, and simplify complex scientific/medical information ... remote environment Salary Range: $80K - $85K per year. Flywheel Partners LLC. provides Equal ...

YO IT Consulting

Biology QA Lead - Remote

... scientific writing, technical review, quality control, biotechnology, life sciences, or related ... supporting remote teams of trainers, annotators, reviewers, researchers, technical writers ...

YO IT Consulting

Biology QA Lead - Remote

... scientific writing, technical review, quality control, biotechnology, life sciences, or related ... moving remote environments using tools such as Discord, Google Sheets, Google Docs, trackers ...

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Remote Scientific Writing information

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$70.5K

$79.5K

How much do remote scientific writing jobs pay per year?

As of Jul 16, 2026, the average yearly pay for remote scientific writing in the United States is $70,499.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,000.00 and $74,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Remote Scientific Writing position, and why are they important?

To thrive in Remote Scientific Writing, you need strong research, analytical, and technical writing skills, usually backed by a degree in a scientific discipline. Familiarity with reference management software like EndNote or Mendeley, as well as proficiency in formatting and submitting manuscripts for scientific journals, is often required. Being detail-oriented, self-motivated, and possessing excellent communication skills are important soft skills for this role. These abilities are critical for producing clear, accurate, and publishable scientific documents while working independently and meeting tight deadlines remotely.

What are some typical daily responsibilities for a Remote Scientific Writing position?

In a Remote Scientific Writing role, your daily tasks often include researching scientific literature, drafting and editing manuscripts, and ensuring documents adhere to specific journal or publication guidelines. You may also collaborate remotely with researchers, editors, and subject matter experts to clarify technical content or gather additional data. Adhering to deadlines and managing multiple projects at once are common aspects of this role. Regular communication through email, project management tools, and virtual meetings is essential for coordination and feedback, even while working independently.

What is a Remote Scientific Writing job?

A Remote Scientific Writing job involves creating and editing scientific content, such as research papers, grant proposals, regulatory documents, or educational materials, from a remote location. Writers typically work for research institutions, pharmaceutical companies, or scientific publishers. This role requires strong writing skills, domain-specific knowledge, and the ability to communicate complex scientific concepts clearly. Many remote scientific writers have advanced degrees in science, medicine, or engineering.

More about Remote Scientific Writing jobs
What cities are hiring for Remote Scientific Writing jobs? Cities with the most Remote Scientific Writing job openings:
What are the most commonly searched types of Scientific Writing jobs? The most popular types of Scientific Writing jobs are:
What states have the most Remote Scientific Writing jobs? States with the most job openings for Remote Scientific Writing jobs include:
What job categories do people searching Remote Scientific Writing jobs look for? The top searched job categories for Remote Scientific Writing jobs are:
Remote Scientific Writing jobs near you
Infographic showing various Remote Scientific Writing job openings in the United States as of July 2026, with employment types broken down into 90% Full Time, 7% Part Time, and 3% Contract. Highlights an 40% Physical, 3% Hybrid, and 57% Remote job distribution, with an average salary of $70,499 per year, or $33.9 per hour.
Associate Director, Medical Writer

Associate Director, Medical Writer

MannKind Corporation

Bedford, MA • On-site, Remote

$148K - $222K/yr

Full-time

Posted 3 days ago

Job description

MannKind Corporation is a biopharmaceutical company dedicated to transforming chronic disease care through innovative, patient‑centric solutions, developing and commercializing innovative inhaled therapeutics and drug‑device technologies aimed at addressing serious unmet needs across endocrine, cardiorenal, and orphan lung diseases. The company applies deep expertise in formulation science and inhalation‑device engineering to reduce the treatment burden for conditions such as diabetes, congestive heart failure, pulmonary fibrosis, and pulmonary hypertension.

MannKind’s core technologies, including ultrafine dry‑powder formulations and advanced inhalation platforms, enable rapid, convenient delivery of medicines directly to the deep lung. This approach supports both local pulmonary targeting and systemic delivery for various medical indications. Through alternative drug formulations and delivery mechanisms, MannKind aims to bring forward differentiated, patient‑centric therapies that expand treatment options to improve outcomes across chronic and rare diseases.
At MannKind, our employees are our greatest asset. We foster a close-knit, collaborative culture where every team member plays a vital role in our mission. We are proud to champion a rich blend of backgrounds, perspectives, and working styles as we work together to improve health outcomes and change lives.
Position Summary:
MannKind Corporation is seeking a detail-oriented and highly organized Medical Writer to join our team. The Medical Writer will provide advanced scientific writing expertise and ensure the successful preparation of high-quality documents including but not limited to study protocols, CSRs, DSURS, IB, safety narratives, publications and submission documents. This role involves providing medical writing support for multiple compounds and projects within multiple therapeutic areas, potentially interfacing with external groups, and serving as the scientific writing expert for the department.
Essential Duties and Job Functions:
  • Coordinate and lead the review, approval, and production of writing projects, arranging and driving review meetings with cross-functional teams.
  • Ensure effective communication among project team members and contributors, holding them accountable to agreed-upon project dates.
  • Leads strategic document preparation for INDs, NDAs and briefing documents
  • Establish best practices, workflow infrastructure/templates, and standards to enhance consistency and quality across all regulatory and scientific documents.
  • Oversee the development and finalization of high-quality, scientifically accurate, ICH-compliant documents, including clinical study protocols and reports, Investigator Brochures, Periodic Safety Updates, patient narratives, and manuscripts for peer-reviewed publications.
  • Stay abreast of global regulatory requirements and guidelines (FDA, EMA, PMDA, ICH, etc.), ensuring company compliance and best practices.
  • Partner with cross-functional teams, including clinical development, medical affairs, regulatory affairs, safety to ensure seamless integration of medical writing.
  • Lead and oversee medical writing project timelines, ensuring alignment with broader corporate milestones.
  • Serve as the medical writer representative on project teams.
  • Write and edit scientific, clinical, or abstracts, posters, presentations, digital enhancements, and manuscripts aligned with scientific narrative and objectives.
  • Complete reviews, quality checks and approvals.
  • Summarize results presented in graphical, tabular, and/or listing format.
  • Interpret complex clinical data and convert it into clear, concise, and engaging scientific content for diverse audiences.
Knowledge, Experience and Skills:
  • BS/BA +12 / MS/MBA 8-10, PhD 5+
  • Degree in science or medical related field. Master’s or PhD preferred.
  • Minimum of 7 years relevant industry experience in medical writing in sponsor/CRO setting or academia, or related areas such as quality, regulatory submissions, publications, clinical research, or product support/R amp;D.
  • Knowledge of US and international regulations, requirements, and guidance associated with writing projects.
  • Excellent written and oral communication skills, attention to detail, and ability to correct errors in spelling, punctuation, grammar, consistency, clarity, and accuracy.
  • Extensive experience working with collaborative, cross-functional teams
  • Develop and/or update document templates, work instructions, style guides, and department-related processes (SOPs)
  • Experience working on publications for multiple therapeutic areas, endocrinology and pulmonology preferred.
  • Understanding of publication/scientific communication guidelines.
  • Ability to provide strategic oversight while managing multiple priorities in a fast-paced environment.
  • Deep understanding of ICH-GCP guidelines and other relevant regulatory requirements.
  • Strategic thinker with strong execution skills.
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