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Clinical Research Protocol Writer Jobs (NOW HIRING)

Houston Methodist

... team as written in the research protocol. Contributes to teamwork by consistently responding ... Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards ...

Houston Methodist

... team as written in the research protocol. Contributes to teamwork by consistently responding ... Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards ...

Houston Methodist

... team as written in the research protocol. Contributes to teamwork by consistently responding ... Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards ...

Houston Methodist

... team as written in the research protocol. Contributes to teamwork by consistently responding ... Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards ...

McLaren

Coordinator Clinical Research

Flint, MI · On-site

$23.50 - $31.25/hr

... research protocol to the medical and nursing staff; evaluating the eligibility of potential ... Essential Functions and Responsibilities : 1. Evaluates eligibility of candidates for clinical ...

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Clinical Research Protocol Writer information

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$54

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How much do clinical research protocol writer jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for clinical research protocol 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 are the primary responsibilities of a Clinical Research Protocol Writer on a daily basis?

As a Clinical Research Protocol Writer, your key daily responsibilities include drafting, reviewing, and revising clinical trial protocols to ensure scientific accuracy and regulatory compliance. You will also collaborate closely with cross-functional teams such as clinical scientists, regulatory affairs, and project managers to gather input and integrate feedback into protocol documents. Managing timelines, maintaining version control, and staying updated on changing regulatory guidelines are also important aspects of the role. This position requires balancing multiple projects and maintaining high standards of quality and clarity in all written materials.

What is a Clinical Research Protocol Writer job?

A Clinical Research Protocol Writer is responsible for drafting detailed documents that outline the objectives, design, methodology, and procedures of clinical research studies. They collaborate with researchers, regulatory teams, and sponsors to ensure protocols comply with regulatory requirements and ethical guidelines. Their work is critical in securing approvals from institutional review boards (IRBs) and regulatory agencies like the FDA. Strong writing skills, knowledge of clinical trial regulations, and attention to detail are essential for this role.

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

To thrive as a Clinical Research Protocol Writer, you need a strong understanding of clinical research methodology, regulatory requirements, and scientific writing, often supported by a background in life sciences or related fields. Familiarity with document management systems, protocol templates, and guidelines such as GCP, ICH, and FDA regulations is highly beneficial. Excellent attention to detail, organizational skills, and the ability to distill complex information into clear, concise documents set candidates apart. These competencies ensure protocols are accurate, compliant, and actionable, which is crucial for supporting successful clinical trials.

More about Clinical Research Protocol Writer jobs
What are the most commonly searched types of Clinical Research Protocol Writer jobs? The most popular types of Clinical Research Protocol Writer jobs are:
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Clinical Research Protocol Writer jobs near you
Infographic showing various Clinical Research Protocol Writer job openings in the United States as of June 2026, with employment types broken down into 98% Full Time, and 2% Part Time. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $113,048 per year, or $54.4 per hour.
Clinical Research Specialist

Clinical Research Specialist

Touro University

Hawthorne, NY • On-site

$75/hr

Part-time

Posted 25 days ago

Touro University rating

5.9

Company rating: 5.9 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

491st of 537 rated colleges and universities

Job description

Overview
Consultant for clinical research protocol enrollment and management.
Responsibilities
  • To perform and provide consultation for investigator initiated and cooperative group basic, translational and clinical research in cellular therapy and stem cell transplantation.
  • Participate in relevant clinical research protocol patient consenting/enrollment in conjunction with the physician PIs and clinical research team
  • Provide oversight for clinical trial data integrity.

Qualifications
Cellular therapy and hematopoietic stem cell transplantation studies.
Maximum Salary
USD $75.00/Hr.

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