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Remote Science Writer Internship Jobs in Beaverton, OR

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 ...

Actuarial Internship

Portland, OR · Remote

$23.50 - $26.50/hr

Work in our flexibility-first environment that combines the best parts of remote work with an ... Preferred majors in Actuarial Science, Mathematics, Statistics, or related field * Strong ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

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Remote Science Writer Internship information

See Beaverton, OR salary details

$22

$49

$76

How much do remote science writer internship jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for remote science writer internship in Beaverton, OR is $49.03, according to ZipRecruiter salary data. Most workers in this role earn between $35.00 and $61.01 per hour, depending on experience, location, and employer.

What is a remote science writer internship?

A Remote Science Writer Internship is a position where interns work from home or another remote location to create, edit, and review science-related content. Interns may write articles, summaries, reports, or social media posts about scientific topics, often translating complex research into accessible language for a wider audience. This type of internship offers valuable experience in scientific communication, research, and writing, and is typically suited for students or recent graduates with a background in science and an interest in journalism or science communication.

What are the key skills and qualifications needed to thrive as a remote science writer intern?

To thrive as a Remote Science Writer Intern, you need strong writing, research, and analytical skills, often supported by a background in science or journalism. Familiarity with citation styles, scientific databases, and content management systems is typically required. Exceptional communication, attention to detail, and time management are crucial soft skills for standing out in this role. These skills ensure accurate, engaging, and timely science communication to a broad audience in a remote work environment.

What are some common challenges faced by remote science writer interns, and how can they be addressed?

Remote science writer interns often face challenges such as managing time effectively across different projects, staying motivated without in-person supervision, and ensuring clear communication with editors and team members. To overcome these, it's helpful to establish a structured daily routine, set clear deadlines, and utilize collaboration tools like Slack or Trello for regular updates. Additionally, proactively seeking feedback and participating in virtual meetings can foster connection and support professional growth.

What is the difference between Remote Science Writer Internship vs Remote Science Content Coordinator?

AspectRemote Science Writer InternshipRemote Science Content Coordinator
Required CredentialsRelevant science degree or coursework, writing samplesSimilar credentials, often with additional project management skills
Work EnvironmentRemote, internship setting, entry-levelRemote, coordinating content teams, more experienced
Employer & Industry UsageResearch institutions, science media, publishingScientific organizations, media outlets, educational platforms
Search & Comparison IntentEntry-level science writing roles, internshipsContent management, team coordination roles

The Remote Science Writer Internship focuses on developing writing skills in a remote setting for those starting their science communication careers. In contrast, the Remote Science Content Coordinator involves managing and coordinating content creation, requiring more experience. Both roles are remote and industry-specific, but they differ in responsibilities and career level.

What are popular job titles related to Remote Science Writer Internship jobs in Beaverton, OR?

For Remote Science Writer Internship jobs in Beaverton, OR, the most frequently searched job titles are:

What job categories do people searching Remote Science Writer Internship jobs in Beaverton, OR look for?

The top searched job categories for Remote Science Writer Internship jobs in Beaverton, OR are:

What cities near Beaverton, OR are hiring for Remote Science Writer Internship jobs?

Cities near Beaverton, OR with the most Remote Science Writer Internship job openings:

Senior Staff Medical Writer (Remote)

Stryker

Portland, OR • On-site, Remote

$143K - $238K/yr

Full-time

Posted 5 days ago


Stryker rating

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

131st of 494 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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