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Remote International Surgeon Jobs (NOW HIRING)

Stryker

Senior Staff Medical Writer (Remote)

Seattle, WA · On-site +1

$143K - $238K/yr

... surgery through brilliant visualization, connected OR solutions, sports medicine products to ... Knowledge of clinical operations, risk management, and international regulatory requirements.

New

Stryker

Senior Staff Medical Writer (Remote)

Phoenix, AZ · On-site +1

$143K - $238K/yr

... surgery through brilliant visualization, connected OR solutions, sports medicine products to ... Knowledge of clinical operations, risk management, and international regulatory requirements.

New

Stryker

Senior Staff Medical Writer (Remote)

Denver, CO · On-site +1

$143K - $238K/yr

... surgery through brilliant visualization, connected OR solutions, sports medicine products to ... Knowledge of clinical operations, risk management, and international regulatory requirements.

Stryker

Senior Staff Medical Writer (Remote)

Portland, OR · On-site +1

$143K - $238K/yr

... surgery through brilliant visualization, connected OR solutions, sports medicine products to ... Knowledge of clinical operations, risk management, and international regulatory requirements.

New

Mizuho OSI

Country Manager, Brazil

Union City, CA · Remote

$110K/yr

Remote opportunity based in Brazil. About Company Mizuho OSI is the leader in the markets for ... The company's portfolio includes specialty surgical tables for procedure-specific approaches that ...

Mizuho OSI

Country Manager, Brazil

Union City, CA · Remote

$110K/yr

Remote opportunity based in Brazil. About Company Mizuho OSI is the leader in the markets for ... The company's portfolio includes specialty surgical tables for procedure-specific approaches that ...

STG International

REMOTE Dietitian - PT

$32.70/hr

This can be REMOTE but must be licensed in state of NY. JOB SUMMARY: Clinic Dietitian at the VA ... Completes comprehensive pre- and post-surgery assessment of bariatric surgery candidates. • ...

STG International

REMOTE Dietitian - PT

Potsdam, NY · On-site +1

$32.70/hr

This can be REMOTE but must be licensed in state of NY. JOB SUMMARY: Clinic Dietitian at the VA ... Completes comprehensive pre- and post-surgery assessment of bariatric surgery candidates. • ...

Joint Commission

Surveyor - Ambulatory Care MD

$171K/yr

Overview Nationwide Search - Incumbent can be located anywhere in the United States Seeking Surgeon ... international flight routes and facilities capable of accommodating wide-body aircraft. #LI-REMOTE ...

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Showing results 21-40

All Jobsremote JobsHealthcare JobsDoctors JobsGeneral Surgeon JobsRemote International Surgeon Jobs

Remote International Surgeon information

See salary details

$38K

$339.2K

$400K

How much do remote international surgeon jobs pay per year?

As of Aug 21, 2026, the average yearly pay for remote international surgeon in the United States is $339,174.00, according to ZipRecruiter salary data. Most workers in this role earn between $303,000.00 and $400,000.00 per year, depending on experience, location, and employer.

What is the difference between Remote International Surgeon vs Remote Medical Consultant?

AspectRemote International SurgeonRemote Medical Consultant
Required CredentialsMedical degree, surgical license, board certificationMedical degree, specialization, often board-certified
Work EnvironmentOperates remotely for consultations, planning, and case reviews; may collaborate with hospitals abroadProvides expert advice, reviews cases, develops protocols remotely for healthcare organizations
Employer & Industry UsageHospitals, clinics, telemedicine platforms worldwideHealthcare consulting firms, hospitals, telehealth companies

Remote International Surgeons and Remote Medical Consultants both require medical credentials and often work in telemedicine settings. Surgeons focus on surgical planning and remote consultations, while Medical Consultants provide expert advice and protocol development. Both roles serve global healthcare providers but differ mainly in their clinical versus advisory focus.

More about Remote International Surgeon jobs

What cities are hiring for Remote International Surgeon jobs?

Cities with the most Remote International Surgeon job openings:

What are the most commonly searched types of International Surgeon jobs?

The most popular types of International Surgeon jobs are:

What states have the most Remote International Surgeon jobs?

States with the most job openings for Remote International Surgeon jobs include:

What job categories do people searching Remote International Surgeon jobs look for?

The top searched job categories for Remote International Surgeon jobs are:

Remote International Surgeon jobs near you
Infographic showing various Remote International Surgeon job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $339,174 per year, or $163.1 per hour.

Senior Staff Medical Writer (Remote)

Stryker

Los Angeles, CA • On-site, Remote

$143K - $238K/yr

Full-time

Posted 3 days ago

New

Stryker rating

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

130th of 493 rated machine equipment manufacturers

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.

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