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Writing Online Remote 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 ... Drive continuous improvement initiatives, maintain medical writing tools and templates, and mentor ...

First Page Sage

$70K - $75K/yr

You should have professional writing experience in several of the following areas: * Cybersecurity ... Reliable internet connection and dedicated remote workspace. Duties: * Leverage proprietary AI ...

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What is a writing online remote job?

Online remote writing jobs are positions where individuals create written content for clients or companies while working from a location of their choice, rather than a traditional office. These roles can include blogging, copywriting, technical writing, content creation, and editing. Remote writers often communicate with clients or employers via email, chat, or project management tools, and they may work as freelancers or as part of a company's remote team. These jobs provide flexibility in terms of schedule and workplace, making them appealing for people who want to work from home or travel.

What are the key skills and qualifications needed to thrive as an online remote writer?

To thrive as an Online Remote Writer, you need excellent writing, grammar, and research skills, often supported by a relevant degree or portfolio of published work. Familiarity with content management systems (CMS) like WordPress, SEO tools, and editing software is typically required. Strong time management, adaptability, and clear communication are essential soft skills for managing deadlines and collaborating virtually. These skills ensure that writers produce high-quality, engaging content efficiently while meeting the needs of clients or audiences in a remote environment.

What are some common challenges faced by writers working in online remote positions, and how can they be managed?

Writers in online remote roles often encounter challenges such as managing deadlines across different time zones, maintaining clear communication with editors or clients, and staying motivated without direct supervision. To overcome these, it's helpful to establish a consistent work schedule, use project management tools for tracking tasks, and participate in regular virtual check-ins with the team. Proactively seeking feedback and clarifying expectations can also help ensure work aligns with project goals and reduces misunderstandings.

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Senior Staff Medical Writer (Remote)

Stryker

Denver, CO • On-site, Remote

$143K - $238K/yr

Full-time

Posted 20 days ago

Stryker rating

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

134th of 499 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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