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Remote Senior Science Writer Jobs in California (NOW HIRING)

Kleinfelder Inc

Senior Electrical Engineer

Concord, CA · On-site +1

$118K - $153K/yr

Step into Your New Role We are looking to hire a full-time hybrid or remote Senior Electrical ... Partner with stakeholders in proposal writing, marketing presentations, and organization of ...

Kleinfelder Inc

Senior Electrical Engineer

Concord, CA · On-site +1

$118K - $153K/yr

Step into Your New Role We are looking to hire a full-time hybrid or remote Senior Electrical ... Partner with stakeholders in proposal writing, marketing presentations, and organization of ...

Veristat

Principal Medical Writer

Ontario, CA · On-site +1

Benefits vary by location and may include: o Remote working o Flexible time off o Paid holidays o ... Bachelor's degree required; science-related field preferred. Minimum of 7 years of medical writing ...

YO AI Labs

AI Data Science Expert - Remote

Palo Alto, CA · Remote

$100 - $200/hr

Remote Job Overview We are seeking experienced AI Data Science Domain Experts to contribute their ... Technical & Report Writing * Content Review & Editing * Data Annotation * Data Interpretation

YO AI Labs

AI Data Science Expert - Remote

San Jose, CA · Remote

$100 - $200/hr

Remote Job Overview We are seeking experienced AI Data Science Domain Experts to contribute their ... Technical & Report Writing * Content Review & Editing * Data Annotation * Data Interpretation

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All JobsScience Writer JobsRemote Senior Science Writer JobsRemote Senior Science Writer Jobs in California

Remote Senior Science Writer information

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.

What are popular job titles related to Remote Senior Science Writer jobs in California?

For Remote Senior Science Writer jobs in California, the most frequently searched job titles are:

What job categories do people searching Remote Senior Science Writer jobs in California look for?

The top searched job categories for Remote Senior Science Writer jobs in California are:

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Cities in California with the most Remote Senior Science Writer job openings:

Remote Senior Science Writer jobs near you
Infographic showing various Remote Senior Science Writer job openings in California as of June 2026, with employment types broken down into 1% Internship, 5% As Needed, 27% Full Time, 64% Part Time, 2% Temporary, and 1% Nights. Highlights an 76% Physical, 3% Hybrid, and 21% Remote job distribution.

Sr. Manager, Medical Writing (Remote)

San Diego, CA • On-site, Remote

Artiva Biotherapeutics, Inc.
Biotechnology Research and Development • 11 - 50 employees
Learn more about Artiva Biotherapeutics, Inc.external

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 10 days ago

Job description

About Artiva:
We are a clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies. Our mission is to develop effective, safe, and accessible cell therapies for patients with devastating autoimmune diseases. We aim to develop therapies that patients and physicians can utilize in a community setting. Our lead product candidate, AlloNK®, is a non-genetically modified, cryopreserved NK cell therapy being evaluated in combination with B-cell targeted monoclonal antibodies (mAbs). We believe the compelling cell killing properties of NK cells, when combined with mAbs for targeting, creates an opportunity to generate potentially transformative therapies.
For more information, visit www.artivabio.com.
Job Summary:
The Sr. Manager, Medical Writing plays a key role in supporting clinical development, regulatory submissions, and scientific communications across Artiva Biotherapeutics. Reporting to the Associate Director, Medical Writing, this individual is a capable, hands-on author of clinical and regulatory documents and a reliable contributor across cross-functional teams. The ideal candidate brings practical experience leading and preparing clinical and regulatory documents, a working knowledge of ICH/GCP and global regulatory expectations, and the ability to deliver clear, scientifically rigorous documents on tight timelines. This role has no direct reports and helps ensure that medical writing deliverables meet the highest scientific, editorial, and compliance standards through cross-functional collaboration with Clinical Development, Clinical Operations, Regulatory Affairs, Biometrics, and Pharmacovigilance.
DUTIES/RESPONSIBILITIES:
  • Author clinical and regulatory documents, including clinical study protocols and amendments, Investigator Brochures, lab manuals, annual reports (e.g., DSURs/IND annual reports), clinical study reports, and clinical sections of regulatory submissions (IMPDs, INDs, CTAs, and BLAs/MAAs as applicable).
  • Write, edit, and collaborate with members of the clinical development team on a variety of clinical and regulatory documents, ensuring scientific accuracy, internal consistency, and compliance with established standards.
  • Support efficient document management and apply a consistent style of presentation to maintain quality and ease of review across documents assembled in a regulatory dossier.
  • Apply established standards and best practices for the document review, completion, and approval process; ensure adherence to regulatory requirements and guidelines, where applicable.
  • Collaborate with the team to develop and maintain medical writing standards, including document templates and style guides.
  • Review and edit documents or sections of documents prepared by functional area representatives and ensure adherence to established standards.
  • Author and coordinate high-quality written responses to health authority questions and deficiency letters in collaboration with Regulatory Affairs and other cross-functional partners.
  • Plan, write, edit, and review materials in collaboration with project teams, including conference abstracts, posters, oral presentations, and manuscripts, ensuring alignment with scientific strategies and corporate goals.
  • Coordinate and prioritize multiple project deadlines in a fast-paced environment; create and maintain timelines for assigned projects.
  • Perform quality review of documents in compliance with established standards and best practices and contribute to the overall quality of the medical writing program.

PROFESSIONAL EXPERIENCE/QUALIFICATIONS
  • Bachelor's degree required; advanced degree (MS, PhD, PharmD, or equivalent) preferred in Biology, Chemistry, Biochemistry, or a related life science discipline.
  • Four or more years' experience preparing clinical and regulatory documents in a life science organization, including late-stage development experience (e.g., CSRs, BLA/MAA clinical sections).
  • Experience supporting cell therapy, gene therapy, or biologics programs is strongly preferred.
  • Demonstrated ability to author and edit clinical-regulatory documents (e.g., protocols, IBs, CSRs, ICFs, briefing documents, and clinical sections of CTAs/INDs/IMPDs) with minimal supervision.
  • Working knowledge of ICH/GCP guidelines, FDA and EMA expectations for clinical-regulatory documents, and applicable editorial standards.
  • Experience supporting health authority interactions, including preparation of briefing documents and written responses to agency questions, is preferred.
  • Strong analytical, written, and editorial skills; ability to communicate complex scientific concepts clearly and concisely.
  • Strong organizational skills and attention to detail; ability to manage multiple projects and competing deadlines in a fast-paced, dynamic environment.
  • Ability to work effectively with internal and outsourced teams and to develop productive working relationships with key cross-functional stakeholders, including Clinical Development, Clinical Operations, Regulatory Affairs, Biometrics, and Pharmacovigilance.

In addition to a great culture, we offer:
  • A beautiful facility
  • An entrepreneurial, highly collaborative, and innovative environment
  • Comprehensive benefits, including:
  • Medical, Dental, and Vision
  • Group Life Insurance
  • Long Term Disability (LTD)
  • 401(k) Retirement Plan
  • Employee Assistance Program (EAP)
  • Flexible Spending Account (FSA)
  • Paid Time Off (PTO)
  • Company paid holidays, including the year-end holiday week
  • Our recognition program, Bonus.ly, is where you can trade in points earned for things you want.

If all this speaks to you, come join us on our journey!
Base Salary: $165,000 - 180,000. Exact compensation may vary based on skills and experience.

Apply