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Contractual Clinical Research Protocol Writer Jobs

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 ...

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 ...

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Contractual Clinical Research Protocol Writer information

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$54

$83

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

As of Aug 11, 2026, the average hourly pay for contractual 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.

Is a contractual clinical research protocol writer an entry level job?

A contractual clinical research protocol writer is typically an experienced role that requires specialized knowledge of clinical trial processes, regulatory requirements, and medical writing skills. While some entry-level positions may exist, most contracts prefer candidates with prior experience or relevant certifications such as GCP or ICH guidelines.

What is the difference between Contractual Clinical Research Protocol Writer vs Clinical Research Associate?

AspectContractual Clinical Research Protocol WriterClinical Research Associate
Primary RoleDevelops and writes clinical trial protocols and related documentsMonitors clinical trials, ensures compliance, and manages site activities
Required SkillsScientific writing, regulatory knowledge, protocol developmentMonitoring, site management, data collection
Work EnvironmentOffice-based, often freelance or contractOn-site at clinical trial sites or remotely
Industry UsagePharmaceutical, biotech, CROsPharmaceutical, biotech, CROs

While both roles are essential in clinical research, Contractual Clinical Research Protocol Writers focus on creating detailed trial protocols, whereas Clinical Research Associates oversee trial conduct and compliance. Understanding these differences helps in choosing the right career path or job search focus.

Who writes contractual clinical research protocols?

Contractual clinical research protocols are typically written by clinical research protocol writers or specialists, often with backgrounds in clinical research, regulatory affairs, or medical writing. They collaborate with investigators, sponsors, and regulatory teams to develop detailed plans that outline study objectives, procedures, and compliance requirements.
What cities are hiring for Contractual Clinical Research Protocol Writer jobs? Cities with the most Contractual Clinical Research Protocol Writer job openings:
What are the most commonly searched types of Clinical Research Protocol Writer jobs? The most popular types of Clinical Research Protocol Writer jobs are:
What states have the most Contractual Clinical Research Protocol Writer jobs? States with the most job openings for Contractual Clinical Research Protocol Writer jobs include:
Contractual Clinical Research Protocol Writer jobs near you
Infographic showing various Contractual Clinical Research Protocol 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 Research Specialist

Touro University

Hawthorne, NY • On-site

$75/hr

Part-time

Re-posted 22 days ago

Touro University rating

5.9

Company rating: 5.9 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

569th of 617 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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