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Review Writer Jobs in Remote, OR (NOW HIRING)

TechData Service Company LLC

Medical Writer (Remote)

OR · Remote

$85 - $90/hr

Medical Writer Contract Position - 6 months with potential extension Position Summary Our client is ... Key Responsibilities Author, review, and edit clinical and regulatory documents, including ...

MyFlorida

CONTRACT MANAGER SPECIALIST - 60072675

OR

$60K/yr

... writing, contract management, evaluation, and closeout. REQUIREMENTS Essential Job Functions ... Responsible for the review, development, and implementation of policies, procedures, standards, and ...

SDLC Technologies

Be Seen First

Content Analyst (Master's Degree Mandatory)

OR · Remote

$21/hr

Excellent written, Verbal Communication and Interpersonal skills including familiar with local ... Ensure the accuracy and timeliness of data feeds and flows for the process and produces, reviews ...

Costco Wholesale Corporation

Cake Decorator

Roseburg, OR · On-site

$13.50 - $17.25/hr

Please click here to review the Costco Applicant Privacy Notice. The jobs listed are examples of ... Cuts, fills and ices cakes. Decorates and writes messages on cakes using pastry bags and tips.

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How much do review writer jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for review writer in Remote, OR is $38.90, according to ZipRecruiter salary data. Most workers in this role earn between $28.80 and $47.07 per hour, depending on experience, location, and employer.

What is a Review Writer job?

A Review Writer is responsible for evaluating products, services, or experiences and composing detailed, unbiased reviews. They research subjects thoroughly, test or analyze items when applicable, and provide honest and informative content for readers. Review Writers may work for media outlets, blogs, or companies that require consumer feedback. Strong writing skills, attention to detail, and the ability to present balanced opinions are essential for this role.

What are the key skills and qualifications needed to thrive in the Review Writer position, and why are they important?

To thrive as a Review Writer, strong writing skills, attention to detail, and a good grasp of grammar and style are essential, often supported by a background in English, journalism, or communications. Familiarity with content management systems (CMS), SEO tools, and sometimes review platforms like Trustpilot is beneficial. Creativity, adaptability, and the ability to meet tight deadlines are valuable soft skills for producing engaging, timely reviews. These skills ensure the production of high-quality, credible content that informs readers and supports the publication's reputation.

What are typical daily responsibilities for a Review Writer?

As a Review Writer, your daily tasks typically include researching products, services, or experiences, composing detailed and unbiased reviews, and editing content for clarity and accuracy. You may collaborate closely with editors or other writers and sometimes attend briefings or product demonstrations. Meeting deadlines and adapting your writing style to fit different audiences or platforms are also common. This variety makes the role dynamic and offers opportunities to expand your expertise across different topics and industries.

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Review Writer jobs near you
Medical Writer (Remote)

Medical Writer (Remote)

TechData Service Company LLC

OR • Remote

$85 - $90/hr

Contractor

Medical, Dental

Posted 17 days ago

Job description

Company: Biotechnology Company

Title: Medical Writer

Contract Position - 6 months with potential extension

Position Summary
Our client is seeking an experienced Medical Writer to develop high-quality clinical and regulatory documents in support of clinical development and regulatory submissions. This role will partner with Clinical Development, Regulatory Affairs, Biostatistics, Medical Affairs, Quality Assurance, and external vendors to produce clear, accurate, and compliant documents.
Key Responsibilities
Author, review, and edit clinical and regulatory documents, including protocols, protocol amendments, clinical study reports, investigator’s brochures, informed consent forms, CTD clinical modules, briefing documents, safety reports, and responses to regulatory questions.
Support clinical development activities by helping prepare clinical development plans, protocols, and related study documents.
Interpret complex clinical and scientific data and communicate findings clearly and accurately.
Ensure documents comply with ICH, GCP, FDA, EMA, and other applicable regulatory guidelines.
Collaborate with cross-functional teams to manage document timelines, review cycles, and submission-ready deliverables.
Review documents prepared by internal teams or external vendors for clarity, consistency, scientific accuracy, and regulatory compliance.
Qualifications
Advanced degree preferred, such as PhD, PharmD, MD, or MSc in Life Sciences, Medicine, Pharmacy, or a related field.
Minimum 3–5 years of medical writing experience in the pharmaceutical, biotech, or CRO industry.
Strong experience writing clinical trial and regulatory submission documents.
Knowledge of drug development, clinical research, clinical study conduct, regulatory requirements, and biostatistical concepts.
Familiarity with medical terminology and coding dictionaries such as MedDRA and WHODrug.
Strong knowledge of ICH/GCP and regulatory submission requirements.
Epilepsy or neurology experience is a plus.
Veeva experience preferred.
Proficiency with Microsoft Word, Excel, PowerPoint, Adobe Acrobat, EndNote, and document management systems.
Ideal Candidate
The ideal candidate is a detail-oriented medical writer who can manage multiple projects, work independently, collaborate effectively with cross-functional teams, and produce clear, well-structured, submission-ready clinical and regulatory documents.

Company Description

www.techdataservice.com