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Clinical Writer Jobs (NOW HIRING)

SGS

Clinical Writer I

Richardson, TX · On-site

Writes and reviews ICH/GCP-adherent clinical study protocols, coordinates internal and external reviews, and obtains client agreement by project deadline * Drafts clinical study reports based on ...

SGS U.S. Holding Inc.

Clinical Writer I

Richardson, TX · On-site

Writes and reviews ICH/GCP-adherent clinical study protocols, coordinates internal and external reviews, and obtains client agreement by project deadline * Drafts clinical study reports based on ...

MMS

Senior Nonclinical Writer (US)

Boston, MA · On-site

This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position. Roles and Responsibilities: * Strong ...

MMS

Senior Nonclinical Writer (US)

Canton, MI · On-site

This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position. Roles and Responsibilities: * Strong ...

MMS

Senior Nonclinical Writer (US)

Raleigh, NC · On-site

This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position. Roles and Responsibilities: * Strong ...

Vaxcyte

Director, Clinical Medical Writing

San Carlos, CA · On-site +1

$221K - $258K/yr

Experience as lead writer for key documents included in major US and/or international regulatory ... Clear understanding of clinical development, including the phases, processes, and techniques used ...

Mercor

Clinical Trial Writer - PhD

San Francisco, CA · Remote

$90 - $150/hr

Medical Writer Type: Contract Compensation: $90-$150/hour Location: Remote Commitment: 20-25 hours/week Role Responsibilities * Generate and validate high-quality, synthetic clinical trial data.

YO AI Labs

Clinical Document Author - Remote

Atlanta, GA · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview We are seeking an experienced Medical Writer / Clinical Document Author to develop ...

YO AI Labs

Clinical Document Author - Remote

Houston, TX · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview We are seeking an experienced Medical Writer / Clinical Document Author to develop ...

YO AI Labs

Clinical Document Author - Remote

Boston, MA · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview We are seeking an experienced Medical Writer / Clinical Document Author to develop ...

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Clinical Writer information

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How much do clinical writer jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for clinical writer in the United States is $54.35, according to ZipRecruiter salary data. Most workers in this role earn between $39.90 and $64.18 per hour, depending on experience, location, and employer.

What is a clinical writer?

A Clinical Writer is a professional who creates, edits, and manages medical and scientific documents related to clinical research, healthcare, and pharmaceuticals. They often prepare clinical study reports, regulatory submissions, patient information leaflets, and scientific manuscripts. Clinical Writers work closely with researchers, physicians, and regulatory professionals to ensure that complex clinical information is communicated clearly, accurately, and in compliance with industry standards. Their work is essential for documenting clinical trials and supporting the approval of new drugs or therapies.

What are the key skills and qualifications needed to thrive as a clinical writer?

To thrive as a Clinical Writer, you need a solid background in life sciences or medical fields, excellent writing skills, and attention to detail, often supported by a relevant degree. Familiarity with regulatory guidelines, literature databases, and tools like EndNote, as well as certifications such as AMWA or EMWA, are highly valued. Strong communication, critical thinking, and time management help Clinical Writers convey complex information clearly and collaborate with medical professionals. These skills ensure the accuracy, clarity, and compliance of clinical documents critical for regulatory submissions and advancing medical knowledge.

What are some common challenges clinical writers face when translating complex medical research into accessible documents?

Clinical writers often encounter the challenge of interpreting highly technical and data-rich research while ensuring accuracy and regulatory compliance. Balancing the need for scientific precision with the ability to communicate information clearly to various audiences—such as healthcare professionals, regulatory agencies, or patients—requires strong analytical and communication skills. Additionally, clinical writers must stay updated on evolving guidelines and collaborate closely with subject matter experts, which can be demanding but also enriches their expertise and professional network.

Do clinical writers make good money?

Clinical 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 skills or certifications in regulatory writing or medical communications.

How can I get into clinical writing with no experience?

Clinical writers typically need strong writing skills, a background in life sciences or healthcare, and familiarity with regulatory guidelines. Gaining experience through internships, entry-level medical writing roles, or certification programs like the American Medical Writers Association can help build relevant skills and credibility for entry into the field.

Is there a demand for clinical writers?

There is a steady demand for clinical writers in the healthcare and pharmaceutical industries due to the need for clear documentation of clinical trial data, regulatory submissions, and medical communications. Opportunities are available in biotech, pharmaceutical companies, and contract research organizations, often requiring knowledge of regulatory guidelines and scientific writing skills.
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Clinical Writer jobs near you
Infographic showing various Clinical Writer job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $113,048 per year, or $54.4 per hour.

Clinical Writer I

SGS

Richardson, TX • On-site

Full-time

Re-posted 11 days ago

Job description

Company Description
We are SGS - the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.
Job Description
  • Drafts protocols and reports for clinical studies on cosmetics or other claims.
  • Uses internal or client template, study outline, clinical data, International Council on Harmonisation (ICH) and Good Clinical Practice (GCP) guidelines, and other relevant information.
  • Coordinates internal and external protocol reviews and obtains client agreement
  • Writes and reviews ICH/GCP-adherent clinical study protocols, coordinates internal and external reviews, and obtains client agreement by project deadline
  • Drafts clinical study reports based on internal or client template according to clinical data, protocol and amendments and deviations; revises reports based on reviews by quality assurance, statistics department, investigators, client, and others
  • Assists in maintaining internal databases of protocol and report templates, bioinstrumentation specifications, clinical grading parameters, and client preferences
  • Assists in drafting and editing Standard Operating Procedures (SOPs) and Work Instructions (WI) for department as assigned
  • Completes training within required deadline
  • Adheres to internal standards, policies, and procedures

Qualifications
  • Bachelor's degree (technical writing, English, or science preferred).
  • 0-4 years technical writing experience
  • Strong technical writing and editing skills including internal document consistency,
  • Organizational ability, research skills, attention to detail, and the ability to establish priorities with minimal supervision
  • Microsoft Word: Intermediate proficiency (including table creation)
  • Microsoft Excel: Intermediate proficiency

Additional Information
SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.
This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time.
If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call 201-508-3149 for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.

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