Portland, OR · On-site +1
$143K - $238K/yr
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
Portland, OR · On-site +1
$143K - $238K/yr
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
OR · On-site +1
See Yourself at Telix The Medical Writer will contribute to the achievement of Telix's strategic goals by leading and driving the writing process. This role will be responsible for planning and
OR · On-site +1
See Yourself at Telix The Medical Writer will contribute to the achievement of Telix's strategic goals by leading and driving the writing process. This role will be responsible for planning and
Lead Technical Writer, Clinical AI/ML amp; SaMD We are seeking a Lead Writer to partner closely with a Program Manager in developing high-stakes federal proposals (e.g., ARPA-H, BARDA, SBIR) for
Lead Technical Writer, Clinical AI/ML amp; SaMD We are seeking a Lead Writer to partner closely with a Program Manager in developing high-stakes federal proposals (e.g., ARPA-H, BARDA, SBIR) for
Albany, OR · On-site
$60K - $70K/yr
Proven to Perform. From the edges of space to the bottoms of ocean, our materials are proven to perform -- and so is our team. We're hiring high performers as proven as our products. Join us. We are
Albany, OR · On-site
$60K - $70K/yr
Proven to Perform. From the edges of space to the bottoms of ocean, our materials are proven to perform -- and so is our team. We're hiring high performers as proven as our products. Join us. We are
Albany, OR · On-site
$54K - $87K/yr
Proven to Perform. From the edges of space to the bottoms of ocean, our materials are proven to perform -- and so is our team. We're hiring high performers as proven as our products. Join us. We are
Albany, OR · On-site
$54K - $87K/yr
Proven to Perform. From the edges of space to the bottoms of ocean, our materials are proven to perform -- and so is our team. We're hiring high performers as proven as our products. Join us. We are
Bend, OR · Remote
$50 - $80/hr
Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project
Bend, OR · Remote
$50 - $80/hr
Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project
Salem, OR · Remote
$50 - $80/hr
Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project
Salem, OR · Remote
$50 - $80/hr
Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project
Beaverton, OR · Remote
$50 - $80/hr
Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project
Beaverton, OR · Remote
$50 - $80/hr
Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project
Portland, OR · Remote
$50 - $80/hr
Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project
Portland, OR · Remote
$50 - $80/hr
Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project
Hillsboro, OR · Remote
$50 - $80/hr
Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project
Hillsboro, OR · Remote
$50 - $80/hr
Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project
Eugene, OR · Remote
$50 - $80/hr
Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project
Eugene, OR · Remote
$50 - $80/hr
Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project
Gresham, OR · Remote
$50 - $80/hr
Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project
Gresham, OR · Remote
$50 - $80/hr
Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project
$60K - $70K/yr
Proven to Perform. From the edges of space to the bottoms of ocean, our materials are proven to perform -- and so is our team. We're hiring high performers as proven as our products. Join us. We are
$60K - $70K/yr
Proven to Perform. From the edges of space to the bottoms of ocean, our materials are proven to perform -- and so is our team. We're hiring high performers as proven as our products. Join us. We are
Portland, OR · On-site
$125K - $170K/yr
MULTIPLE POSITIONS AVAILABLE Employer: AMAZON DEVELOPMENT CENTER U.S., INC., Offered Position: Tech Writer-Tech III Job Location: Portland, Oregon Job Number: AMZ10358499 Position Responsibilities:
Portland, OR · On-site
$125K - $170K/yr
MULTIPLE POSITIONS AVAILABLE Employer: AMAZON DEVELOPMENT CENTER U.S., INC., Offered Position: Tech Writer-Tech III Job Location: Portland, Oregon Job Number: AMZ10358499 Position Responsibilities:
* This position is primarily remote but may require 1 day on-site * * JOB SUMMARY/PURPOSE * Supports research and analytic projects across Samaritan Health Services. Collaborates closely with a
* This position is primarily remote but may require 1 day on-site * * JOB SUMMARY/PURPOSE * Supports research and analytic projects across Samaritan Health Services. Collaborates closely with a
Corvallis, OR · On-site
* This position is primarily remote but may require 1 day on-site * * JOB SUMMARY/PURPOSE * Supports research and analytic projects across Samaritan Health Services. Collaborates closely with a
Corvallis, OR · On-site
* This position is primarily remote but may require 1 day on-site * * JOB SUMMARY/PURPOSE * Supports research and analytic projects across Samaritan Health Services. Collaborates closely with a
$11.6K - $18.2K
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$70.9K - $77.5K
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$77.6K is the 75th percentile. Wages above this are outliers.
$77.5K - $84.1K
26% of jobs
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A Science Writer researches, writes, and edits content about scientific topics for various audiences. They translate complex scientific information into clear and engaging articles, reports, or scripts for publications, websites, and media outlets. Science Writers may work for universities, research organizations, media companies, or as freelancers. Their work helps bridge the gap between scientists and the public by making scientific discoveries and advancements accessible and understandable.
To thrive as a Science Writer, you need a solid background in scientific concepts, strong research abilities, and exceptional writing and editing skills, often supported by a degree in science or journalism. Familiarity with citation management tools, content management systems, and scientific databases is usually required. Attention to detail, creativity, and the ability to communicate complex ideas clearly are essential soft skills that set outstanding candidates apart. These competencies are crucial for crafting accurate, engaging, and accessible content that effectively bridges the gap between scientific experts and the general public.
Science Writers often encounter the challenge of translating complex scientific concepts into clear, compelling language for a broader audience without compromising accuracy. They must stay up-to-date with the latest research and frequently juggle tight deadlines while coordinating with subject matter experts and editors. Additionally, working in a fast-paced environment sometimes requires quick adaptation to new topics or publication formats. Overcoming these challenges sharpens communication skills, broadens subject expertise, and builds a portfolio of diverse, high-impact work.
The most popular types of Science Writer jobs in Oregon are:
For Science Writer jobs in Oregon, the most frequently searched job titles are:
The top searched job categories for Science Writer jobs in Oregon are:
Cities in Oregon with the most Science Writer job openings:
For Science Writer jobs in OR, the most frequently searched job titles are:
Portland, OR • On-site, Remote
$143K - $238K/yr
Full-time
Posted 27 days ago
Author and maintain clinical and regulatory documentation such as Clinical Evaluation Reports (CERs) and Post-Market Clinical Follow-Up (PMCF) documents.
Compile, analyze, and synthesize clinical evidence from various sources into submission-ready regulatory documents.
Collaborate with cross-functional teams to develop clinical evidence strategies, regulatory documentation plans, and project timelines.
8.2
Based on 113 frontline employees who took The Breakroom Quiz
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:
Sourced by ZipRecruiter
Medical equipment and supplies manufacturing
10,000+ Employees
Kalamazoo, MI, US
