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Remote Report Writer Jobs in Colorado (NOW HIRING)

Stryker

Senior Staff Medical Writer (Remote)

Denver, CO · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Author and maintain Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-Up (PMCF ...

New

micro1 AI

Medical Writing Manager

Boulder, CO · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

micro1 AI

Medical Writing Manager

Lakewood, CO · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

micro1 AI

Medical Writing Manager

Thornton, CO · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

micro1 AI

Medical Writing Manager

Westminster, CO · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

micro1 AI

Medical Writing Manager

Arvada, CO · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

micro1 AI

Medical Writing Manager

Centennial, CO · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

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Remote Report Writer information

What is a remote report writer?

A Remote Report Writer is a professional who creates, edits, and formats reports for organizations while working from a remote location, such as their home. They analyze data, organize information, and present findings in clear, concise documents tailored to the needs of their clients or employers. Remote Report Writers may work in various fields, including business, healthcare, education, or technology, and often use specialized software to compile and present data. Strong writing, analytical, and communication skills are essential for this role.

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

To thrive as a Remote Report Writer, you need strong written communication, analytical skills, and attention to detail, often supported by a relevant degree in English, communications, or a related field. Familiarity with word processing software, data visualization tools, and sometimes content management systems is typically required. Excellent time management, self-motivation, and the ability to collaborate virtually are vital soft skills in this remote setting. These competencies ensure that reports are accurate, clear, and delivered on time, enabling effective decision-making for stakeholders.

How does a remote report writer typically collaborate with subject matter experts and other team members while working remotely?

As a Remote Report Writer, collaboration with subject matter experts and colleagues is usually facilitated through digital communication tools like email, video calls, and project management platforms. You may be expected to attend virtual meetings to clarify project objectives, gather technical details, and review drafts. Building clear lines of communication and being proactive in seeking feedback are essential, as you won't have immediate in-person access to your team. Effective remote collaboration ensures that your reports are accurate, comprehensive, and tailored to the audience's needs.

What is the difference between Remote Report Writer vs Remote Content Writer?

AspectRemote Report WriterRemote Content Writer
Primary FocusCreating detailed reports, data analysis, and summariesProducing articles, blog posts, and marketing content
Required SkillsData analysis, report formatting, technical writingCreative writing, SEO, audience engagement
Work EnvironmentOften in corporate, finance, or research settingsTypically in marketing, media, or online publishing
Common CertificationsNone mandatory, but technical or data analysis certifications helpNone required, but writing or SEO certifications are advantageous

While both roles involve writing, Remote Report Writers focus on data-driven reports and technical summaries, often within corporate or research environments. Remote Content Writers create engaging online content aimed at audiences and marketing goals. Understanding these differences helps job seekers target the right opportunities based on their skills and interests.

What are the most commonly searched types of Report Writer jobs in Colorado?

The most popular types of Report Writer jobs in Colorado are:

What are popular job titles related to Remote Report Writer jobs in Colorado?

For Remote Report Writer jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Remote Report Writer jobs in Colorado look for?

The top searched job categories for Remote Report Writer jobs in Colorado are:

What cities in Colorado are hiring for Remote Report Writer jobs?

Cities in Colorado with the most Remote Report Writer job openings:

Remote Report Writer jobs near you

Senior Staff Medical Writer (Remote)

Stryker

Denver, CO • 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.

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