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Senior Staff Medical Writer (Remote)

Stryker

Remote · USJob$110–238K/yrPosted 1 day agoSeen in employer's feed today

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At a glance

Compensation
$110–238K/yr
Location
Remote · US
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Requirements

Credentials this posting asks for.

Master's degree

Job overview

Stryker is hiring a Senior Staff Medical Writer in its Neurovascular Division for a remote U.S. position. The role leads clinical evidence strategies and scientific documentation supporting regulatory submissions, market access, and product lifecycle decisions. It partners with regulatory, research and development, clinical, marketing, and quality teams to evaluate and communicate evidence, and mentors team members while improving clinical evaluation methods and documentation practices.

Skills & qualifications

RequiredNice to have

Skills

Clinical Evidence StrategyClinical EvaluationLiterature ReviewsEvidence SynthesisScientific AnalysisRegulatory SubmissionsProduct Lifecycle ManagementGlobal Regulatory RequirementsCross-Functional Project Management

Qualifications

Master's in Related Science6+ Years Relevant Experience2+ Years Medical Device Clinical Evaluation ExperienceDoctoral Degree or Equivalent

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match

Full job description

Stryker is hiring a Senior Staff Medical Writer for our Neurovascular Division . This is a remote position within the United States.

As the Senior Staff Medical Writer , you will lead the development of clinical evidence strategies and scientific documentation that support regulatory submissions, market access initiatives, and product lifecycle decisions. This position partners closely with Regulatory Affairs, Research and Development, Clinical, Marketing, and Quality teams to ensure clinical evidence is effectively evaluated, communicated, and applied throughout the product lifecycle.

What You Will Do

  • Lead the development and execution of clinical evidence strategies for new product development and lifecycle management activities.

  • Manage clinical evaluation projects, ensuring alignment between clinical evidence, regulatory strategy, product claims, and commercialization objectives.

  • Author and maintain clinical evaluations, post-market clinical follow-up documentation, regulatory submissions, annual reports, and other clinical documentation.

  • Design and execute systematic literature reviews, evaluate published evidence, and synthesize clinical, preclinical, and post-market data into scientifically supported conclusions.

  • Assess benefit-risk profiles of medical devices and develop evidence-based recommendations in accordance with global regulatory requirements.

  • Partner with regulatory authorities and internal stakeholders to address clinical evidence requirements and support regulatory submissions.

  • Develop scientific communications, including manuscripts, conference abstracts, presentations, white papers, and customer-facing evidence materials.

  • Mentor team members, lead cross-functional review processes, and identify opportunities to improve clinical evaluation methodologies, documentation practices, and team efficiency.

What You Need

Required

  • Master of Science degree in a health, clinical, biological science, biomedical, engineering, or related scientific field.

  • Minimum 6 years of experience in clinical affairs, regulatory affairs, quality, medical writing, clinical evaluation, post-market surveillance, or related field.

  • Minimum 2 years of experience authoring clinical evaluations for medical devices.

  • Experience conducting literature reviews, evidence synthesis, and scientific analysis using clinical and/or technical data.

  • Experience supporting regulatory submissions and product lifecycle activities within a regulated healthcare industry.

Preferred

  • Doctoral degree (PhD, PharmD, MD, or equivalent) in a health or science-related discipline.

  • Experience supporting global medical device regulatory requirements, including clinical evaluation, post-market clinical follow up, and market access activities.

  • Experience applying global regulatory requirements, including ISO, FDA, and international regulations

  • Experience managing complex cross-functional projects within the medical device industry.

Posted Date: 11/04/2026

This role will be posted for a minimum of 3 days.

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 (https://view.stryker.com/viewer/fcd609f31e39eac44598615224ec7216?iid=69deda99678eb495e0710914#1) to find the pay range for your location.

Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.

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.

How this job compares

Set against the 996 open Regulatory Affairs jobs on Olive Jobs, counted November 5, 2026.

Pay
  • This posting$110–238K/yr
  • California median$150–204K/yr114 salary ranges
  • US median$142–201K/yr658 salary ranges

This range's midpoint, $174K, is close to the California median midpoint ($172K) — in the middle half of Regulatory Affairs salary ranges in California.

Openings
Olive Jobs lists 143 open Regulatory Affairs jobs in California and 996 across the US. 15% of them nationwide are listed as remote or flexible.
Hiring the most in California
Experience
This posting asks for at least 6 years of experience; Regulatory Affairs postings that state a minimum ask for 7 years at the median (864 postings).
Education
This posting asks for a master's degree; 138 of the 996 open Regulatory Affairs jobs (14%) ask for a master's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 5, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

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