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Remote Science Writer Jobs in Riverside, CA (NOW HIRING)

CellCarta

Scientific Writer

Lake Forest, CA · On-site +1

$30 - $35/hr

Scientific Writer Are you ready to launch your career in the exciting world of clinical trials and biotech? We're seeking a driven and detail-oriented Scientific Writer to join our dynamic team. This ...

Corvel

Data Science Manager

Irvine, CA · On-site +1

This position is open to remote or hybrid. ESSENTIAL FUNCTIONS & RESPONSIBILITIES: * Design, build ... Ability to write, review, and optimize Python and SQL code * Deep understanding of Large Language ...

Corvel

Data Scientist II

Irvine, CA · On-site +1

$82.57K - $127.49K/yr

... written/verbal communication skills EDUCATION & EXPERIENCE: * Bachelor's degree in Computer Science ... Remote Equal Opportunity Employer This employer is required to notify all applicants of their ...

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$16

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$61

How much do remote science writer jobs pay per hour?

As of May 28, 2026, the average hourly pay for remote science writer in Riverside, CA is $36.63, according to ZipRecruiter salary data. Most workers in this role earn between $24.33 and $53.17 per hour, depending on experience, location, and employer.

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

A Remote Science Writer needs strong scientific literacy, excellent writing skills, and typically a degree in a scientific discipline or journalism. Familiarity with reference management tools, content management systems, and style guides such as APA or AMA is common. Attention to detail, time management, and the ability to communicate complex ideas clearly are standout soft skills. These abilities ensure the accurate, engaging, and timely delivery of scientific information to diverse audiences in a remote work environment.

How do Remote Science Writers typically collaborate with researchers and editors while working offsite?

Remote Science Writers often use digital communication tools such as email, video conferencing, and project management platforms to coordinate with researchers, editors, and other team members. Regular check-ins and virtual meetings help clarify scientific concepts, align on content expectations, and ensure accuracy and clarity in the writing. Writers may also participate in online editorial reviews and use collaborative document platforms to receive feedback and track revisions. This structure fosters a supportive environment despite the physical distance, enabling writers to contribute effectively to multi-disciplinary projects.

What is a remote science writer?

A remote science writer is a professional who creates articles, reports, or content about scientific topics while working from a location outside of a traditional office, often from home. Their responsibilities include researching scientific developments, interviewing experts, and translating complex scientific information into clear, accessible language for various audiences. Remote science writers may work for media outlets, research institutions, educational organizations, or as freelancers. This role requires strong writing skills, scientific literacy, and the ability to work independently while meeting deadlines.

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

AspectRemote Science WriterRemote Scientific Content Editor
CredentialsBachelor's or higher in science, writing experienceSimilar credentials, with additional editing or proofreading experience
Work EnvironmentRemote, freelance or full-timeRemote, often part of a publishing or research team
Employer & IndustryResearch institutions, science publications, biotech companiesScientific journals, publishing houses, research organizations
Search & Comparison IntentWriting-focused roles, content creationEditing, quality control, content refinement

Remote Science Writers focus on creating original scientific content, while Remote Scientific Content Editors review and refine existing material. Both roles require strong scientific knowledge and writing skills, but editors emphasize editing and quality assurance. Understanding these differences helps job seekers find roles aligned with their skills and career goals.

What are the most commonly searched types of Science Writer jobs in Riverside, CA? The most popular types of Science Writer jobs in Riverside, CA are:
What are popular job titles related to Remote Science Writer jobs in Riverside, CA? For Remote Science Writer jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Remote Science Writer jobs in Riverside, CA look for? The top searched job categories for Remote Science Writer jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Remote Science Writer jobs? Cities near Riverside, CA with the most Remote Science Writer job openings:
Remote Science Writer jobs near you
Infographic showing various Remote Science Writer job openings in Riverside, CA as of May 2026, with employment types broken down into 63% Full Time, 33% Part Time, and 4% Contract. Highlights an 29% Physical, 42% Hybrid, and 29% Remote job distribution, with an average salary of $76,199 per year, or $36.6 per hour.

Scientific Writer

CellCarta

Lake Forest, CA • On-site, Remote

$30 - $35/hr

Temporary

Posted 13 days ago

Job description

Scientific Writer
Are you ready to launch your career in the exciting world of clinical trials and biotech? We're seeking a driven and detail-oriented Scientific Writer to join our dynamic team. This entry-level role offers the opportunity to gain hands-on experience and grow your expertise in a fast-paced, innovative environment. As a key member of our team, you will have the opportunity to work with cutting-edge technology, collaborate with cross-functional teams, and gain valuable experience. Get ready to take your first step in a rewarding career in the biotech industry and join us today!
Summary
The Scientific Writer is responsible for writing and quality control (QC) of scientific or technical documentation, including validation reports, clinical trial and non-clinical study reports, data presentations, training guidelines, standard operating procedures (SOPs), and other scientific documentation generated at the CellCarta Lake Forest site. This role also involves writing study plans and analytical plans for client studies and serving as backup to the client services team in preparing study budgets.
Responsibilities
  • Prepare, edit, or review documentation that includes but is not limited to assay validation reports, optimization/characterization reports, clinical and non-clinical study reports, study plans, analytical plans, SOPs, training guidelines, continuing education materials, and presentations.
  • Prepare clear, accurate, and insightful manuscript-style final study, optimization/characterization, and validation reports, which include an introduction, materials and methods, results, discussion, and references. Results may be presented with tables, graphs, statistical analysis, and photomicrographs. Technical document templates are usually available; however, custom reports may be requested.
  • Review study plans/analytical plans and deliverables to ensure that all raw data is available for reports. Report any missing deliverables or documentation to the project manager or assay development scientist.
  • Prepare PowerPoint presentations that may incorporate a synopsis of the study, methods, images, results, and conclusions. Presentations may be prepared for project updates during meetings between assay development scientists and clients for assay development studies. Presentations may also be prepared for project updates during meetings between project managers and clients for clinical and non-clinical studies.
  • Prepare study plans and analytical plans outlining work to be completed for clients in accordance with the study budget. Prepare updates to these documents throughout the study as requested by project managers and assay development scientists in new versions of the document.
  • Perform QC of all documentation types responsible for preparing as process dictates. Provide clear and insightful feedback to ensure the quality of all documentation created by the scientific writing team.
  • Manage and maintain trackers for all deliverable deadlines. Notify supervisor, project manager or assay development scientist, or deliverable requestor in a timely manner of any expected or actual delays.
Education
  • A bachelor's degree in Biology, Biochemistry, Biomedical Sciences, Pharmaceutical Sciences, or Medicine. A master's degree is preferred, but not required.
Qualification and Skills
  • 1-2 years of relevant scientific/technical writing experience.
  • Experience with histopathology, anatomic pathology, and immunohistochemistry (IHC) is strongly preferred. Knowledge of genomics, FISH, ISH, immunofluorescence is a plus but not required.
  • Ability to produce high-quality scientific content with precision and clarity.
  • Attention to detail in grammar, formatting, referencing, and scientific accuracy, with a commitment to maintaining consistency across documents and projects.
  • Ability to work with cross-disciplinary teams. Strong communication and interpersonal skills.
  • Some experience in managing multiple concurrent projects with competing deadlines, ensuring timely delivery of high-quality deliverables in a fast-paced, client-driven setting.
  • Ability to organize and effectively present validation, clinical, and non-clinical data using tables, figures, and visual tools that meet scientific and regulatory standards.
  • Comfortable using document management systems and writing tools (Microsoft Office suite) and statistical analysis methods.
  • Knowledge of regulatory requirements and relevant QA guidelines.
Working Conditions
  • Part time: 20-25 hours / week
  • Temporary: 6 months
  • Hybrid: flexibility to work from home.
What we can offer
CellCarta is made up of dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world!
Our Offerings
  • Competitive wages: $30-35 / hour
  • Sick time
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The Company operates globally with facilities located in Canada, USA, Belgium, Australia, and China.
Joining CellCarta means working with dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world!
Join us as we make an impact on patient therapy!
The information collected to review your application will be processed by the human resources services of CellCarta Biosciences Inc. and its affiliates (collectively, "CellCarta"). The legal basis for this processing is the legitimate interest of CellCarta to evaluate the suitability of candidates for the roles available at CellCarta.
CellCarta will only process that information which is necessary to evaluate your application. This information includes identifying information such as your name, address, email address and phone number, as well as information about your education and professional experience, including previous positions and your CV. Such information is required for us to complete your applicant file, assess your suitability for the role and comply with applicable laws. CellCarta may obtain personal information from other sources, such as during reference, background, or employment checks, with your permission, and from third party sources such as recruitment and assessment sites or professional social media sites, in each case only if such information is relevant to reviewing your application. Your personal information will be retained only for so long as reasonably necessary and in accordance with applicable laws. This information will be processed confidentially and only accessed by those who have a need for the recruitment process. Please note that the information comprising your applicant file may be processed in a country that is not where you are located (for example, you might be in the European Economic Area or Québec, Canada, whereas your applicant file may be reviewed by CellCarta in the United States). If you are offered and accept employment with CellCarta Biosciences Inc. or one of its affiliates, the information collected will become part of your employment record. If you do not want us to retain your information, or want us to update it, please contact [email protected].

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