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Hourly Clinical Research Protocol Writer Jobs (NOW HIRING)

TriHealth, Inc.

Clinical Research Nurse

Cincinnati, OH

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Demonstrates the ability to develop processes to facilitate implementation of the research protocol ... Acts as the point person for audit staff coming into institution for a review prepares a written ...

TriHealth, Inc.

Clinical Research Nurse

Cincinnati, OH

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Demonstrates the ability to develop processes to facilitate implementation of the research protocol ... Acts as the point person for audit staff coming into institution for a review prepares a written ...

University of Miami

Clinical Research Coordinator 1

Miami, FL · On-site

$23.25 - $30.75/hr

  • Medical

  • Dental

Maintains enrollment procedures according to the protocol. 2. Coordinates routine activities of ... Ensures data integrity and consistency in computer database and written records by reviewing ...

Avispa Technology

Clinical Research Coordinator

Palo Alto, CA · On-site

$45 - $50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Hourly pay: $45-$50/hr * Worksite: Leading university (Palo Alto, CA 94304 - Hybrid) * W2 ... Monitor study conduct and operational activities to ensure compliance with research protocols ...

Wisconsin

Clinical Research Coordinator

Madison, WI · On-site

$24.50 - $32.50/hr

  • Retirement

  • PTO

... study protocol. Our team of clinical research coordinators and research nurses apply expertise ... Effective oral and written communication skills * Ability to manage multiple projects at the same ...

Cape Fox Corporation

Research Nurse

Bethesda, MD · On-site

$56/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The total hourly pay for this exempt position is $56.00 for up to 40 hours per week. This rate ... writers on the production/revision of clinical research protocols * Support the needs of data ...

Cape Fox SS

Research Nurse

Bethesda, MD

$56/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The total hourly pay for this exempt position is $56.00 for up to 40 hours per week This rate ... writers on the production/revision of clinical research protocols Support the needs of data ...

University of Miami

Clinical Research Coordinator 2

Miami, FL

$23.25 - $30.75/hr

  • Medical

  • Dental

This role assists in the day-to-day operations of clinical research protocol implementation, and carries out study coordination duties from protocol initiation to study close-out according to ...

Cape Fox Corporation

Research Nurse

Baltimore, MD · On-site

$45 - $50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Recruits and screens patients for inclusion in protocols and clinical trials. * Assist research and ... written. * Excellent analytical, organizational and time management skills. The total hourly pay ...

InStride Health

Clinical Research Scientist

$106K - $118K/yr

... protocol development, study implementation, and regulatory compliance activities including ... Outstanding written and verbal communication skills, including scientific writing and presentation ...

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Showing results 41-60

All JobsHourly Clinical Research Protocol Writer Jobs

Hourly Clinical Research Protocol Writer information

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$25

$54

$83

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

As of Aug 17, 2026, the average hourly pay for hourly 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 is the difference between Hourly Clinical Research Protocol Writer vs Clinical Research Associate?

AspectHourly Clinical Research Protocol WriterClinical Research Associate
CredentialsBachelor's degree in life sciences; experience in protocol writingBachelor's degree; often requires clinical research certifications
Work EnvironmentRemote or office-based; focused on document creationSite visits; monitoring clinical trial progress
Employer & IndustryPharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, clinical trial sites

The main difference is that Hourly Clinical Research Protocol Writers focus on creating and editing trial protocols, while Clinical Research Associates oversee trial conduct and site monitoring. Both roles require knowledge of clinical research processes but serve different functions within the industry.

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Hourly Clinical Research Protocol Writer jobs near you
Infographic showing various Hourly Clinical Research Protocol Writer job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 87% In-person, and 13% Remote job distribution, with an average salary of $113,048 per year, or $54.4 per hour.

Research Intern

Tranquil Clinical Research

Webster, TX • On-site

Other

Re-posted 18 days ago

Job description

Please do not call our office - we will reach out to you.
Description
The Research Intern is an entry level clinical research position. The Intern will perform a variety of research, database and clerical duties of a routine and technical nature to support clinical trials and assist investigators to organize, gather and compile clinical research data. The Intern will primarily be responsible for the collection, aggregation, and analysis of data. The Research Intern will also form other duties such as data entry, and administrative duties such as filing, record keeping, photocopying, and creating flyers/posters. The Research Intern will be supervised by a senior research staff member or principal investigator.
Qualifications
Minimum Education
High School Diploma or GED (Required) Or
Bachelor's Degree May require a Bachelor's degree based on the specific internship program
Minimum Work Experience
0-2 years related experience. 2 years experience working in a medical or scientific research setting, preferred
Required Skills/Knowledge
Demonstrates adherence with the standards for the responsible conduct of research.
Work requires organizational skills, knowledge of basic mathematical, data collection and analysis, and research principles.
Knowledge of human subjects research.
Excellent computer skills in a Windows and/or Mac environment.
Excellent writing, editing, and proofing skills.
Required Licenses and Certifications
CITI Certification (Required)
Valid Driver's license
Functional Accountabilities
Research Projects

  • Maintain confidentiality of data, as required.
  • Plan, conduct and manage research projects.
  • Responsible for appropriate use of research funds and resources.
Project Administration
  • Ensure compliance with program guidelines and requirements of funding and regulatory agencies.
  • Stay informed of and adhere to human research protection guidelines, relevant best practices, and changes to any research protocol.
  • Accurately complete IRB submissions on time.
  • Anticipate study needs and work to accomplish them in a timely manner.
  • Seek assistance, when needed.
Data Collection
  • Collect data in order to facilitate operational and clinical research activities.
  • Enter clinical and research data and information into database, include electronic CRFs and sample tracking databases.
  • Follow established guidelines in the collection of clinical data and/or administration of clinical studies.
  • Support aggregation and analysis of study data, as directed by senior research staff.
Professional Development
  • Attend and contribute to team meetings, including working to set and achieve project timelines and deliverables.
  • Obtain training and certification as required by study protocol (e.g., CITI training).
  • Comply with all annual job-related training requirements.

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