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Scientific Writer Jobs in Arizona (NOW HIRING)

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 ...

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study ...

Onsite POSITION SUMMARY The Content Writer & Producer is responsible for creating clear, compelling ... This role requires a strong ability to balance creative storytelling with scientific accuracy while ...

Technical Writer Primary Skills: Strong Technical Writing Role Description: The Technical Writer ... Bachelor?s degree in computer science or any IT related field. Experience: Minimum 2-3 years of ...

Technical Writer Primary Skills: Strong Technical Writing Role Description: The Technical Writer ... Bachelor's degree in computer science or any IT related field. Experience: Minimum 2-3 years of ...

Our mission is to deliver high-quality service and technology solutions - rooted in strong science ... Write and edit clinical development documents, including but not limited to, clinical protocols ...

... Writer to join our customer in Phoenix, AZ. Please find below additional details about this job ... Bachelor's degree in Computer Science or equivalent (minimum 5 years experience in Information ...

Strong scientific writing, literature evaluation, and communication skills. * Ability to manage multiple priorities while collaborating across cross-functional teams. Preferred * Four or more years ...

Technical Writer - SAP Documentation (Simple Explanation) Location: Tolleson, AZ (100% Onsite) Duration: 06-months contract (may extend) Schedule: Monday-Friday, 8:00 AM-5:00 PM What You'll Do * Talk ...

Proposal Writer Duties and Responsibilities: • Write and Edit Proposals: Effectively convey information about prospective client needs and PR campaigns, understanding and presenting the nuances of ...

Technical Writer (Tempe, AZ - Local Only) Summary The Technical Writer creates, updates, and reviews documents related to the activities of transmission and generation operations. Documents may ...

Technical Writer Job Details Researches, analyzes, designs, develops, writes, edits, and publishes documentation for the Workday Human Capital System using effective Business Process Management (BPM ...

Philanthropy Writer As a key member of the Writing Services team, the Philanthropy Writer works collaboratively with ASUF and ASU leadership, faculty, staff and development colleagues to write, edit ...

They are seeking a Technical Writer who will be responsible for creating and reviewing Knowledge Management content to enhance the customer experience and ensure consistency across business units.

The Technical Writer is responsible for driving a seamless Customer Experience through writing clear and consistent Knowledge Management content. * This position will write and review procedural ...

Service Writer Job Posting | RWC Group | Heavy Duty Commercial Truck & Bus Dealership Keep Commercial Trucks Moving. Deliver an Exceptional Customer Experience. At RWC Group , our Service Writers are ...

Job Title: Technical Writer Location: Phoenix, AZ / Salt Lake City, UT / Ft. Lauderdale, FL Duration: 5 month (may extend) The Technical Writer is responsible for driving a seamless Customer ...

Service Writer Job Posting | RWC Group | Heavy Duty Commercial Truck & Bus Dealership Keep Commercial Trucks Moving. Deliver an Exceptional Customer Experience. At RWC Group, our Service Writers are ...

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Scientific Writer information

See Arizona salary details

$10.3K

$65.7K

$74.1K

How much do scientific writer jobs pay per year?

As of Sep 1, 2026, the average yearly pay for scientific writer in Arizona is $65,698.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,400.00 and $69,000.00 per year, depending on experience, location, and employer.

What is a scientific writer?

A science writer is a journalist who specializes in writing about scientific fields, with an emphasis on the emergence of research and advancements. Science writing is one of the most challenging forms of journalism because you must carefully translate scientific wording about discoveries into terms that the layman can understand while balancing conflicting views from major players in the field. Your responsibilities as a science writer are significant since it's important not to give misinformation to the masses about new research and discoveries. A science writer's day-to-day duties primarily revolve around research, interviews, and writing.

How does a scientific writer typically collaborate with researchers and subject matter experts during the manuscript preparation process?

Scientific Writers work closely with researchers and subject matter experts (SMEs) to ensure technical accuracy and clarity in manuscripts, grant proposals, or regulatory documents. This collaboration often involves interviewing SMEs to clarify complex concepts, reviewing drafts together, and incorporating feedback to meet publication standards. Effective communication and project management skills are essential, as writers must balance scientific rigor with readability, adhere to deadlines, and coordinate input from multiple stakeholders throughout the writing and revision process.

What are the key skills and qualifications needed to thrive as a scientific writer, and why are they important?

To thrive as a Scientific Writer, you need a solid background in science or a related field, excellent writing skills, and typically at least a bachelor’s or master’s degree in a scientific discipline. Familiarity with referencing software (like EndNote or Zotero), publication guidelines, and content management systems is often required. Outstanding attention to detail, the ability to translate complex concepts for different audiences, and strong time-management are standout soft skills. These skills ensure accurate, clear communication of scientific information, which is critical for advancing research and supporting organizational goals.

What is the difference between Scientific Writer vs Medical Writer?

AspectScientific WriterMedical Writer
CredentialsTypically requires a degree in science or related fieldOften requires a degree in life sciences, healthcare, or related fields; certifications like AMWA or EMWA are common
Work EnvironmentResearch institutions, academia, scientific publishingPharmaceutical companies, healthcare organizations, regulatory agencies
Industry UsageUsed across scientific disciplines for research papers, grant proposalsFocused on clinical, regulatory, and medical communication

Scientific Writers and Medical Writers share similar backgrounds in science and often work in related environments. However, Medical Writers specialize in translating complex medical and clinical data for regulatory submissions, medical education, and healthcare audiences, whereas Scientific Writers focus more broadly on scientific research and publications.

How much money do scientific writers make?

Scientific writers typically earn a median annual salary of around $70,000 to $100,000, depending on experience, education, and industry. Salaries can vary based on whether they work as freelancers, in academia, or for private companies, with advanced skills in research and technical writing often commanding higher pay.

Is scientific writing a good career?

Scientific writing is a viable career that involves communicating complex research findings clearly and accurately, often requiring strong writing skills and knowledge of scientific concepts. It offers opportunities in academia, publishing, and industry, with roles that may involve editing, peer review, or content development. Job stability and growth depend on the demand for scientific communication and the ability to adapt to evolving technologies and standards.

What are the most commonly searched types of Scientific Writer jobs in Arizona?

The most popular types of Scientific Writer jobs in Arizona are:

What are popular job titles related to Scientific Writer jobs in Arizona?

For Scientific Writer jobs in Arizona, the most frequently searched job titles are:

What job categories do people searching Scientific Writer jobs in Arizona look for?

The top searched job categories for Scientific Writer jobs in Arizona are:

What cities in Arizona are hiring for Scientific Writer jobs?

Cities in Arizona with the most Scientific Writer job openings:

What are popular job titles related to Scientific Writer jobs in AZ?

For Scientific Writer jobs in AZ, the most frequently searched job titles are:

Infographic showing various Scientific Writer job openings in Arizona as of August 2026, with employment types broken down into 82% Full Time, 15% Part Time, and 3% Contract. Highlights an 75% Physical, 4% Hybrid, and 21% Remote job distribution, with an average salary of $65,698 per year, or $31.6 per hour.

Senior Staff Medical Writer (Remote)

Phoenix, AZ • On-site, Remote


Stryker
Medical Equipment and Supplies Manufacturing • 10K+ employees

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

131st of 495 rated machine equipment manufacturers

Great coworkers

People enjoy working here

Good employer


$143K - $238K/yr

Full-time

Posted 15 days ago


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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