2

Remote Senior Science Writer Jobs in California (NOW HIRING)

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... As the Senior Staff Medical Writer , you will develop scientific and clinical documentation that ...

New

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... As the Senior Staff Medical Writer , you will develop scientific and clinical documentation that ...

New

Senior Manager, Medical Writing

San Diego, CA · On-site +1

  • Medical

  • Life

  • Retirement

  • PTO

San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the ... We continue to courageously forge new paths as we move toward a common goal of elevating science ...

Remote Senior Marketing Specialist

San Diego, CA · Remote

$82K - $102K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

About the Role This is a senior, hands-on role covering email, lifecycle, product, and promotional ... Excellent written and verbal communication, with email content that resonates. * Proven cross ...

New

Remote Senior Marketing Specialist

San Diego, CA · On-site +1

$82K - $102K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

About the Role This is a senior, hands-on role covering email, lifecycle, product, and promotional ... Excellent written and verbal communication, with email content that resonates. * Proven cross ...

New

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study ...

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study ...

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study ...

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study ...

Remote Senior Marketing Specialist

Carlsbad, CA · Remote

$80K - $99K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

About the Role This is a senior, hands-on email and lifecycle marketing role on the arrivia ... Excellent written and verbal communication, with email content that resonates. * Proven cross ...

next page

Showing results 1-20

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 cities in California are hiring for Remote Senior Science Writer jobs?

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

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.

Senior Staff Medical Writer (Remote)

Stryker

San Diego, CA • On-site, Remote

$143K - $238K/yr

Full-time

Posted yesterday

New


Job description

Work Flexibility: Remote

Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based remotely anywhere within the United States. Stryker is one of the world's leading medical technology companies and, together with its customers, is driven to make healthcare better. Our Endoscopy Division delivers a diverse array of innovative medical technologies to support minimal invasive surgery through brilliant visualization, connected OR solutions, sports medicine products to sustainability solutions.

As the Senior Staff Medical Writer, you will develop scientific and clinical documentation that supports global regulatory compliance and market access for medical devices. This position partners closely with Regulatory Affairs, Clinical Affairs, Quality, Research & Development, and Marketing teams to translate complex clinical evidence into high-quality regulatory and scientific documents throughout the product lifecycle.

What You Will Do

  • Author and maintain Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-Up (PMCF) documents, and other clinical evidence documentation supporting international product registrations and lifecycle management.

  • Compile, analyze, and synthesize clinical evidence from clinical studies, published literature, post-market data, and other safety and performance sources into submission-ready regulatory documents.

  • Respond to notified body reviews and regulatory feedback, driving resolution of clinical documentation questions to support ongoing market access.

  • Collaborate with cross-functional teams to develop clinical evidence strategies, regulatory documentation plans, and project timelines.

  • Author clinical study protocols, study reports, data summaries, and supporting scientific documents for regulatory and clinical initiatives.

  • Conduct systematic literature reviews, evaluate scientific data, and integrate findings into clinical and regulatory documentation.

  • Lead document review cycles, coordinate stakeholder feedback, resolve content issues, and obtain timely approvals.

  • Drive continuous improvement initiatives, maintain medical writing tools and templates, and mentor junior medical writing team members.

What You Need

Required

  • Bachelor's degree in a scientific, technical, healthcare, or related discipline.

  • Minimum 6 years of industry experience within medical technology, medical devices, pharmaceuticals, or healthcare products.

  • Minimum 4 years of experience in scientific writing, medical writing, clinical research, or related regulatory documentation activities.

  • Experience authoring Clinical Evaluation Reports (CERs) and Post-Market Clinical Follow-Up (PMCF) documentation.

  • Expert knowledge of MEDDEV 2.7/1 Rev. 4, European Union Medical Device Regulation (EU MDR 2017/745), and Medical Device Coordination Group (MDCG) guidance for clinical evaluations.

  • Experience conducting systematic literature reviews and utilizing scientific databases, literature search methodologies, and literature management tools.

  • Knowledge of FDA, Good Clinical Practice (GCP), ISO 14155, ISO 14971, and applicable international medical device regulations and standards.

Preferred

  • Master's degree, PhD, PharmD, MD, MPH, RN, BSN, or other advanced health-related degree.

  • Experience authoring clinical study protocols, clinical study reports, manuscripts, or scientific publications.

  • Experience supporting regulatory submissions and global market access initiatives for medical devices.

  • Knowledge of clinical operations, risk management, and international regulatory requirements.

United States of America Pay Ranges:

  • USN: $110,100 - $183,400 USD Annual
  • US5: $115,600 - $192,600 USD Annual
  • US10: $121,100 - $201,700 USD Annual
  • US15: $126,600 - $210,900 USD Annual
  • US20: $132,100 - $220,100 USD Annual
  • US30: $143,100 - $238,400 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.

Travel Percentage: 10%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.