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Clinical Protocol Writer Jobs (NOW HIRING)

UAB

CLINICAL RESEARCH COORDINATOR II

Tampa, FL · On-site

$50K - $81K/yr

In conjunction with Investigators, plans and implements the clinical protocol's goals and objectives. * Compiles and edits written reports for both internal and external administrative offices.

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How much do clinical protocol writer jobs pay per hour?

As of Jun 6, 2026, the average hourly pay for clinical 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 key skills and qualifications needed to thrive in the Clinical Protocol Writer position, and why are they important?

To thrive as a Clinical Protocol Writer, you need expertise in clinical research, scientific writing, and regulatory requirements, typically supported by a bachelor's or advanced degree in life sciences or a related field. Familiarity with tools like Microsoft Office, clinical trial management systems (CTMS), and knowledge of ICH-GCP guidelines or similar certifications are highly valued. Strong attention to detail, collaboration skills, and the ability to translate complex scientific concepts into clear, compliant documents set top candidates apart. These skills are essential for generating precise, regulatory-ready protocols that ensure accurate clinical trial execution and cross-team collaboration.

What are the typical daily responsibilities of a Clinical Protocol Writer?

A Clinical Protocol Writer is responsible for drafting and revising clinical trial protocols, ensuring compliance with regulatory guidelines, and incorporating feedback from cross-functional teams such as clinical operations, biostatistics, and regulatory affairs. On a typical day, you may coordinate with investigators, review scientific literature, and attend meetings to discuss study design and objectives. You’ll also manage document version control and ensure timely delivery of protocol drafts and amendments. This role requires balancing independent writing tasks with frequent team collaboration to align clinical documentation with study goals and regulatory standards.

What is a Clinical Protocol Writer job?

A Clinical Protocol Writer is responsible for drafting and developing clinical trial protocols that outline study objectives, methodologies, patient eligibility criteria, and regulatory requirements. They work closely with clinical researchers, regulatory teams, and medical writers to ensure protocols align with industry and compliance standards. Their role is crucial in guiding the execution of clinical trials and ensuring data integrity. Strong writing, attention to detail, and knowledge of regulatory guidelines are essential for success in this role.

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Clinical Protocol Writer jobs near you
Infographic showing various Clinical Protocol Writer job openings in the United States as of May 2026, with employment types broken down into 89% Full Time, and 11% Part Time. Highlights an 51% Physical, 2% Hybrid, and 47% Remote job distribution, with an average salary of $113,048 per year, or $54.4 per hour.
Clinical Research Coordinator (Neurology)

Clinical Research Coordinator (Neurology)

Johns Hopkins University

Baltimore, MD • On-site

$24 - $32/hr

Full-time

Posted 17 days ago

Johns Hopkins Medicine rating

7.5

Company rating: 7.5 out of 10

Based on 200 frontline employees who took The Breakroom Quiz

221st of 867 rated healthcare providers

Job description

The Department of Neurology is seeking a Clinical Research Coordinator who will be responsible for coordinating clinical trials and other clinical research projects for the Johns Hopkins Multiple Sclerosis Center. This may involve, but is not limited to, screening medical records, identifying appropriate patients, consenting study participants, performing data collection and entry, obtaining and processing specimens (e.g., blood, urine), organizing regulatory paperwork.
Specific Duties & Responsibilities
  • Coordinate all activities of a clinical research study to ensure adherence to protocol and validity of findings.
  • Participate in clinical study start-up meetings.
  • Assist research nurses, study coordinators, principal investigators, and other study personnel in executing protocol-related activities.
  • Explain the study background and rationale for the research to potential and current participants
  • Contribute to the development of recruitment strategies for participants for assigned study.
  • Implement a variety of techniques for recruitment as appropriate, e.g., print and web-based advertisements, contact referring physicians, participate in community events, etc.
  • Independently conduct the consenting process or ensure consent is obtained on appropriate participants.
  • Schedule participants for required activities and provide any special instructions prior to upcoming tests/exams.
  • Serve as liaison to study participants.
  • Assist with setup of the data collection system and enter and organize data.
  • Assist in coordinating study meetings.
  • Participate in study meetings and provide updates on protocol implementation status and make recommendations on operational issues.
  • Assist with the preparation of submissions to the Institutional Review Board (IRB)
  • Liaison with IRB on administrative matters and facilitate communications with the PI.
  • Conduct literature searches to provide background information.
  • Obtain and maintain excellent operating knowledge of assigned clinical protocol, clinical equipment, and clinical computer systems.
  • Oversee budget expenditures for study operations.
  • Other duties as assigned.

In additional to the duties above
  • Will be involved in Stiff Person Syndrome Center activities including consenting patients for clinical research and helping with SPS database entry/management.

Minimum Qualifications
  • Bachelor's Degree in a related field.

  • Additional education may substitute for required experience and additional related experience may substitute for required education beyond a high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula.

Preferred Qualifications
  • Related undergraduate or work experience in human subjects research.

Technical Skills & Expected Level of Proficiency
  • Attention to Detail - Awareness
  • Clinical Trial Management System - Awareness
  • Data Entry - Awareness
  • Data Collection and Reporting - Awareness
  • Data Management and Analysis - Awareness
  • Interpersonal Skills - Awareness
  • Oral and Written Communications - Awareness
  • Organizational Skills - Awareness
  • Project Coordination - Awareness
  • Regulatory Compliance - Awareness

The core technical skills listed are most essential; additional technical skills may be required based on specific division or department needs.
Classified Title: Clinical Research Coordinator
Role/Level/Range: ACRO37.5/03/CD
Starting Salary Range: $17.20 - $30.30 HRLY (Commensurate w/exp)
Employee group: Full Time
Schedule: M-F 8:30 am - 5:00 pm
FLSA Status: Non-Exempt
Location: School of Medicine Campus
Department name: SOM Neuro Neuroimmunology
Personnel area: School of Medicine

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