ZipRecruiter

Log In

2

Remote Science Journal Editor Jobs (NOW HIRING)

Advarra

Sr Editor, Consent Form Development

Familiar with Excel, PowerPoint, direct messaging applications such as Slack, remote meeting ... Familiar with scientific/medical terminology and able to convert scientific/medical information to ...

EBSCO

Clinical/Medical Editor II, Critical Care

$68K - $97K/yr

... remote work models. As an AI-enabled service leader, we thrive on innovation, forward-thinking ... scientific content * Demonstrated understanding/use of principles of evidence-based practice and ...

EBSCO

Clinical/Medical Editor II, Critical Care

$68K - $97K/yr

... remote work models. As an AI-enabled service leader, we thrive on innovation, forward-thinking ... scientific content * Demonstrated understanding/use of principles of evidence-based practice and ...

ExtensisHR

Part-time Copyeditor

Manhattan, NY · On-site +1

$30 - $45/hr

Experience editing manuscripts for publication in peer-reviewed academic journals * Experience ... Remote work environment * Project-based workload tied to deadline-driven assessment development ...

next page

Showing results 1-20

All JobsRemote Science Journal Editor Jobs

Remote Science Journal Editor information

See salary details

$11

$31

$57

How much do remote science journal editor jobs pay per hour?

As of Jun 19, 2026, the average hourly pay for remote science journal editor in the United States is $31.60, according to ZipRecruiter salary data. Most workers in this role earn between $21.39 and $39.66 per hour, depending on experience, location, and employer.

How do Remote Science Journal Editors typically collaborate with authors and peer reviewers to ensure the quality of published articles?

Remote Science Journal Editors often work closely with authors and peer reviewers via email, online submission platforms, and virtual meetings. They facilitate communication by providing clear editorial feedback, coordinating revisions, and addressing questions or concerns throughout the review process. Editors also ensure that peer reviewers' comments are constructive and that authors' revisions meet the journal's standards. This collaborative process helps maintain the integrity and scientific rigor of published work, even while working remotely.

What is the difference between Remote Science Journal Editor vs Remote Scientific Writer?

AspectRemote Science Journal EditorRemote Scientific Writer
Required credentialsAdvanced degree in science or related field, editing experienceDegree in science, writing skills, subject expertise
Work environmentAcademic or publishing companies, remoteResearch organizations, publishing, freelance, remote
Employer usageAcademic journals, scientific publishersResearch institutions, publishers, freelance clients
Common search intentEditing, peer review, publication processWriting, research summaries, content creation

The Remote Science Journal Editor primarily focuses on reviewing, editing, and preparing scientific articles for publication, requiring strong editing skills and scientific credentials. In contrast, the Remote Scientific Writer creates original scientific content, research summaries, or articles, emphasizing writing expertise and subject knowledge. Both roles often operate remotely and serve the scientific publishing industry, but their core responsibilities differ significantly.

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

To excel as a Remote Science Journal Editor, you generally need an advanced degree in a scientific field, strong editorial judgment, and experience with scholarly publishing. Familiarity with manuscript submission systems, citation management software, and editing tools like Microsoft Word or LaTeX is typically required. Exceptional attention to detail, strong communication skills, and the ability to manage deadlines set standout editors apart. These competencies are crucial for ensuring the integrity, clarity, and timely publication of scientific research.

What are remote science journal editors?

Remote science journal editors are professionals who manage the peer review and publication process for scientific journals while working from a location outside the traditional office, often from home. Their responsibilities include evaluating manuscript submissions, coordinating with reviewers and authors, making editorial decisions, and ensuring the quality and integrity of published content. Remote work allows these editors to collaborate with international teams and handle submissions from around the world using digital communication tools. This role requires a strong background in science, excellent communication skills, and attention to detail. The position is ideal for those who are organized and can work independently in a virtual environment.
More about Remote Science Journal Editor jobs
What cities are hiring for Remote Science Journal Editor jobs? Cities with the most Remote Science Journal Editor job openings:
What are the most commonly searched types of Science Journal Editor jobs? The most popular types of Science Journal Editor jobs are:
What states have the most Remote Science Journal Editor jobs? States with the most job openings for Remote Science Journal Editor jobs include:
What job categories do people searching Remote Science Journal Editor jobs look for? The top searched job categories for Remote Science Journal Editor jobs are:
Remote Science Journal Editor jobs near you
Infographic showing various Remote Science Journal Editor job openings in the United States as of June 2026, with employment types broken down into 90% Full Time, and 10% Part Time. Highlights an 72% Physical, 4% Hybrid, and 24% Remote job distribution, with an average salary of $65,728 per year, or $31.6 per hour.
Sr Editor, Consent Form Development

Sr Editor, Consent Form Development

Advarra

Remote

Full-time

Medical

Posted 24 days ago

Job description

Company Information
At Advarra, we are passionate about making a difference in the world of clinical research and advancing human health. With a rich history rooted in ethical review services combined with innovative technology solutions and deep industry expertise, we are at the forefront of industry change. A market leader and pioneer, Advarra breaks the silos that impede clinical research, aligning patients, sites, sponsors, and CROs in a connected ecosystem to accelerate trials.
Company Culture
Our employees are the heart of Advarra. They are the key to our success and the driving force behind our mission and vision. Our values (Patient-Centric, Ethical, Quality Focused, Collaborative) guide our actions and decisions. Knowing the impact of our work on trial participants and patients, we act with urgency and purpose to advance clinical research so that people can live happier, healthier lives.
At Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each employee is not only valued but empowered to thrive and make a meaningful impact.
Job Overview Summary
Supports the IRB Services department in the review of incoming submissions and preparation of informed consent forms (ICFs) used in the conduct of human subjects research. In addition, the Senior Editor may mentor new editors and complete projects as defined by management.
Job Duties & Responsibilities
  • Conduct an accurate pre-review of new and revised consent forms in regulatory compliance with applicable FDA, HHS, Health Canada, TCPS2 regulations, ICH GCP guidance, and operational compliance with Advarra Standard Operating Procedures and Work Instructions

  • Edit new and revised consent forms to ensure regulatory compliance and alignment with Advarra operational standards

  • Apply negotiated Sponsor and site language to consent form documents as required by client agreements documented in mandatory language documents or MLD's

  • Collaborate with Board members and staff to include all necessary edits to the consent form from the various stakeholders

  • Complete informed consent quality control check for yourself and others

  • Mentor new team members, as requested

  • Maintain and increase individual regulatory knowledge to assist with organizational compliance:

  • Maintain and increase knowledge of U.S. and/or Canadian Regulations and Guidelines in the area of Human Subject Protections, drug research, device research, and cosmetic research

  • Complete standard Human Subjects Research Training, such as CITI, on a repeating cycle determined by management

  • Complete organizational training as required by management

  • Attend one IRB meeting per month to enhance knowledge and understanding of IRB processes (two meetings per month during the initial training period)

  • Offer process improvement suggestions to management, as applicable

  • Other duties as assigned

Location
This role is open to candidates working remotely in the United States.
Basic Qualifications
  • Minimum of 2 years of experience in technical/medical writing and/or editing in addition to a Bachelor's degree

  • Experience writing and/or editing consent forms or other research documents

  • Proficiency in Word processing and editing (including use of Tracked Changes and Compare Merge functions)

  • Familiar with Excel, PowerPoint, direct messaging applications such as Slack, remote meeting applications such as Zoom or RingCentral, and web-based proprietary software

Preferred Qualifications
  • 1 year of IRB experience

  • Experience writing and/or editing consent forms or other research documents

  • Certified IRB Professional (CIP) or completion of CIP within two (2) years of eligibility

  • Ability to communicate clearly and professional in English, both verbal and written skills

  • Excellent interpersonal skills to work professionally and effectively with others and provide high levels of customer service

  • In-depth knowledge of matters regarding human subjects research and informed consent

  • Familiar with scientific/medical terminology and able to convert scientific/medical information to lay terms

  • Ability to edit technical and/or medical documents

  • Ability to read and comprehend advanced technical/medical documents such as medical protocols and informed consent forms

  • Ability to manage various editing projects under conflicting demands and priorities

  • Dependably produces high quality work

  • Must have high level of attention to detail, accuracy and thoroughness; problem solving skills

  • Ability to follow written and verbal instructions and work independently as required

Physical and Mental Requirements
  • Sit or stand for extended periods of time at stationary workstation

  • Regularly carry, raise, and lower objects of up to 10 Lbs.

  • Learn and comprehend basic instructions

  • Focus and attention to tasks and responsibilities

  • Verbal communication; listening and understanding, responding, and speaking

Advarra is an equal opportunity employer that is committed to providing a workplace that is free from discrimination and harassment of any kind based on race, color, religion, creed, sex (including pregnancy, childbirth, and related medical conditions, sexual orientation, and gender identify), national origin, age, disability or genetic information or any other status or characteristic protected by federal, state, or local law.
Pay Transparency Statement
The base salary range for this role is $66,767 - $116,089. Note that salary may vary based on location, skills, and experience and may vary from the amounts listed above. This position may also be eligible for a variable bonus in addition to base salary as well as health coverage, paid holidays, and other benefits.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
Advarra logo

About Advarra

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

201 - 500 Employees

Headquarters location

Columbia, MD, US

Year founded

1983

Social media

Twitter

View All Advarra Jobs

Apply