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Medical Writer Jobs in Utah (NOW HIRING)

The Medical Writer II collaborates in the development and execution of clinical, scientific, and regulatory documents for global regulatory agencies. This involves collaboration with internal and ...

Medical Writing Manager

Saint George, UT ยท Remote

$50 - $80/hr

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 focused on ...

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 focused on ...

Medical Writing Manager

Provo, UT ยท Remote

$50 - $80/hr

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 focused on ...

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 focused on ...

Medical Writing Manager

West Jordan, UT ยท Remote

$50 - $80/hr

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 focused on ...

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 focused on ...

Medical Billing Specialist

Provo, UT ยท Remote

$50 - $80/hr

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 focused on ...

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 focused on ...

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 focused on ...

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 focused on ...

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Showing results 1-20

Medical Writer information

See Utah salary details

$10

$42

$71

How much do medical writer jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for medical writer in Utah is $42.12, according to ZipRecruiter salary data. Most workers in this role earn between $30.62 and $51.01 per hour, depending on experience, location, and employer.

What is a medical writer?

Medical writers are professionals who create scientific documents related to healthcare, medicine, and the life sciences. They produce materials such as clinical study reports, journal articles, regulatory submissions, and educational content for healthcare professionals or the public. Medical writers must have a strong understanding of medical terminology, research methods, and regulatory guidelines. Their work helps communicate complex scientific information clearly, accurately, and in compliance with industry standards.

What does a medical writer do?

Medical writers create scientific documents and articles. This can include a variety of different types of papers, including research documents, educational or promotional literature, articles, and abstracts. You may ghostwrite for well-known physicians and scientists, or you may write under your own name, depending on what field you are in. Other medical writer jobs include journalists for medical magazines, authors of books, and those who write marketing materials for health care organizations. Regardless of your specialty, you must be able to interpret complex scientific information and create articles that people can read and understand, particularly when writing for the general public.

What skills and qualifications are needed to be a medical writer?

To thrive as a Medical Writer, you need a strong background in life sciences or medicine, excellent written communication skills, and often an advanced degree such as a PhD, MD, or relevant certification. Familiarity with reference management software, medical literature databases, and regulatory guidelines like ICH or GPP is typically required. Attention to detail, the ability to interpret complex data, and collaboration skills set standout professionals apart in this role. These competencies ensure the production of accurate, compliant, and accessible medical documents crucial for regulatory approval, education, and communication in healthcare.

What is the difference between Medical Writer vs Clinical Writer?

AspectMedical WriterClinical Writer
CredentialsTypically requires a degree in life sciences, healthcare, or related fields; certifications like AMWA or EMWA are commonSimilar credentials; often holds degrees in life sciences with certifications in clinical research or writing
Work EnvironmentWorks in pharmaceutical, biotech, or healthcare companies, often in offices or remote settingsPrimarily in clinical research organizations, pharmaceutical companies, or hospitals, often in office or remote settings
Industry UsageUsed across pharma, biotech, medical device industries for regulatory, educational, and promotional contentFocused on clinical trial documentation, protocols, and reports within clinical research

Medical Writers and Clinical Writers share similar backgrounds and work environments, often collaborating in healthcare and pharmaceutical sectors. The main difference lies in their focus: Medical Writers create a broad range of medical content, while Clinical Writers specialize in clinical trial documentation and reports.

Is medical writing a stable career?

Medical writing is generally considered a stable career due to consistent demand for clear communication of scientific and medical information across pharmaceutical, biotech, and healthcare industries. Professionals often require strong writing skills, scientific knowledge, and familiarity with regulatory guidelines, which support long-term employment opportunities. However, job stability can vary based on industry trends, experience, and specialization.

How does a medical writer typically collaborate with subject matter experts during a project?

Medical Writers frequently work closely with physicians, researchers, and regulatory specialists to ensure content accuracy and clarity. This collaboration often involves conducting interviews, reviewing scientific data, and incorporating expert feedback into drafts. Building strong professional relationships and maintaining clear communication are key for efficiently resolving technical questions and aligning final documents with project objectives. This teamwork is essential for producing high-quality, compliant materials that meet both scientific and regulatory standards.
What are the most commonly searched types of Medical Writer jobs in Utah? The most popular types of Medical Writer jobs in Utah are:
What cities in Utah are hiring for Medical Writer jobs? Cities in Utah with the most Medical Writer job openings:
What are popular job titles related to Medical Writer jobs in UT? For Medical Writer jobs in UT, the most frequently searched job titles are:
Infographic showing various Medical Writer job openings in Utah as of August 2026, with employment types broken down into 81% Full Time, and 19% Part Time. Highlights an 100% In-person job distribution, with an average salary of $87,610 per year, or $42.1 per hour.

Medical Writer II

Laborie Medical Technologies Corp

Salt Lake City, UT โ€ข On-site

$115K - $120K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 6 days ago


Job description

We believe that great healthcare is an essential safeguard of human dignity. 

At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact in the lives of patients across the globe, we’d like to meet you.

We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We’re not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion.

Who We’re Looking For: 

The Medical Writer II collaborates in the development and execution of clinical, scientific,

and regulatory documents for global regulatory agencies. This involves collaboration with

internal and external partners to support technical, medical and clinical writing outputs for

Clinical and Regulatory business needs in accordance with the relevant and evolving

international standards as well as LABORIE standard operating procedures. This person

will write a variety of documents for distinct audiences including Post-Market Surveillance

(PMS) plans, PMS reports, Periodic Safety Update Reports (PSURs) and Proactive PMS

study protocols, and will contribute to Clinical Evaluation Reports (CERs) and Post-Market

Clinical Follow-Up Reports (PMCFERs).

About the Role:

• Perform on-line external vigilance reviews and compare results to the Risk

Management File.

• Critically appraise, analyze, and summarize internal and external data in

support of the PMS requirements for geographies such as the EU, Health

Canada, UK, etc.

• Search out, review, write and maintain records of PMS data pertaining to

the safety and effectiveness of Laborie devices.

• Assist in ensuring all PMS requirements are met for device registrations

and maintenance while working with other LABORIE team members.

• Work cross functionally to develop, compile and report proactive PMS activities

and integrate reporting into PMCFERs and PSURs.

• Undertake various projects and tasks as assigned.

What you Bring:

• Bachelor's degree in a scientific field or in writing/composition discipline and 5+

years' experience writing PSURs. Experience with Medical Writing required.

• Working knowledge of medical device clinical and PMS regulations, standards

and guidelines (ISO, MEDDEV, MDR, IVDR, FDA CFR, UKCA, Health Canada) and

experience conducting focused analysis of internal and external complaint data

• Demonstrated ability to manage project timelines, including ability to adapt to

shifting priorities and competing demands while maintaining strong attention to

detail

• Strong computer skills, proficiency with MS Office and ability to work both

independently and collaboratively in a team setting

• Excellent English verbal, written and presentation skills with great attention to

detail

• Experience working in the medical device industry preferred

• Project Management experience preferred

Why Laborie:

Our Mission every day is to operate as a world-class specialist medical company making and advancing technologies that preserve and restore human dignity. We do that today by helping people with pelvic and gastrointestinal conditions live normal lives, and by helping mothers and babies have safe deliveries.

  • Paid time off and paid volunteer time
  • Medical, Dental, Vision
  • Pension Plan
  • Parental Leave and Adoption Services
  • Health and Wellness Programs and Events

Laborie provides equal employment opportunities and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation, or any characteristic protected under applicable law. Laborie is committed to providing access and reasonable accommodation in our services, activities, education, and employment for individuals with disabilities.