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Medical Writer Jobs in Rhode Island (NOW HIRING)

Noblis

Technical Writer

Newport, RI · Hybrid

$44K - $68K/yr

Ensuring written documents are free from grammar, punctuation, and spelling errors. * Gathering ... medical conditions, veteran or military status, or any other characteristics protected by ...

Noblis

Technical Writer

Newport, RI · On-site

Ensuring written documents are free from grammar, punctuation, and spelling errors. * Gathering ... medical conditions, veteran or military status, or any other characteristics protected by ...

Vatn Systems

Technical Writer

Bristol, RI · On-site

Summary Serves as the company's first dedicated technical writer, owning the clarity, consistency, and quality of documentation across the AUV systems integration and test lifecycle. Translates ...

Vatn Systems

Technical Writer

Bristol, RI · On-site

Summary Serves as the company's first dedicated technical writer, owning the clarity, consistency, and quality of documentation across the AUV systems integration and test lifecycle. Translates ...

SEACORP

Technical Writer I

Middletown, RI

The Technical Writer writes and edits proposals; process documentation; technical reports, user ... Medical Benefits: Choice of two medical insurance programs through Blue Cross & Blue Shield.

SEACORP

Technical Writer I

Middletown, RI · On-site

The Technical Writer writes and edits proposals; process documentation; technical reports, user ... Medical Benefits: Choice of two medical insurance programs through Blue Cross & Blue Shield.

SEACORP

Technical Writer I

Middletown, RI · On-site

This role involves writing and editing technical documentation, proposals, and reports while collaborating closely with engineering project teams and subject matter experts. Responsibilities : • ...

SEACORP

Technical Writer I

Middletown, RI · On-site

The Technical Writer writes and edits proposals; process documentation; technical reports, user guides, and procedures; and/or marketing materials for internal use, customer programs, or wider ...

Serco USA

Technical Writer - Remote/Hybrid

Middletown, RI · On-site +1

The Technical Writer will work closely with program personnel and subject matter experts to produce ... Medical, dental, and vision insurance * Robust vacation and sick leave benefits, and flexible work ...

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Medical Writer information

See Rhode Island salary details

$11

$45

$77

How much do medical writer jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for medical writer in Rhode Island is $45.31, according to ZipRecruiter salary data. Most workers in this role earn between $32.98 and $54.86 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.

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 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.

Do medical writers make good money?

Medical writers typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions may start around $60,000 annually, while experienced professionals can earn over $100,000, especially with specialized knowledge or certifications. The role often requires strong writing skills and familiarity with scientific or medical terminology.
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For Medical Writer jobs in Rhode Island, the most frequently searched job titles are:

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Medical Writer jobs near you
Infographic showing various Medical Writer job openings in Rhode Island as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 11% Part Time, and 5% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $94,244 per year, or $45.3 per hour.

Principal Medical Writer - FSP at Parexel Providence, RI

Dart Solutions

Providence, RI • On-site

$110 - $150/hr

Other

Posted 9 days ago

Job description

Principal Medical Writer - FSP job at Parexel. Providence, RI.

Job Summary

The Principal Medical Writer is responsible for writing and overseeing the completion of a broad range of documents in support of company products and projects. This individual will work with the lead and/or program medical writer and independently to develop messages and write, substantively rewrite, and edit documents for clarity and accuracy, ensuring high quality. The individual will help manage project documents and timelines, as well as ensuring that documents comply with International Committee on Harmonization guidelines, SOPs, Good Clinical Practices, and Good Publication Practices. As a study team member, this individual will work with domestic and international colleagues across R&D (as appropriate) to ensure that documents meet the company's objectives.

Key Accountabilities
  • Write and edit clinical regulatory documents for clarity and accuracy according to client standards.
  • Work with lead writer and project team to develop document messages and data presentations within submission timelines to meet company objectives.
  • Provide writing support for a wide range of documents, including but not limited to investigator's brochures, clinical study protocols and reports, integrated summaries, literature reviews, and SOPs.
  • Ensure that documents comply with International Conference on Harmonization guidelines, SOPs, and Good Clinical Practices.
Requirements
  • At least 15 years of medical writing experience in the pharmaceutical industry.
  • Ability to write and edit complex material to ensure accuracy and clarity.
  • Experience with a variety of regulatory and clinical documents.
  • Experience in a matrix team environment.
  • Excellent written and oral communication skills and demonstrated problem‑solving abilities.
  • Ability to handle multiple projects and short timelines.
  • Ability to work cooperatively with colleagues in a wide range of disciplines.
  • Knowledge of ICH and CTD guidelines for clinical and regulatory submission documents.
Education
  • BA/BS, Advanced degree preferred.

EEO DisclaimerParexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

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