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Clinical Protocol Writer Jobs (NOW HIRING)

H. Lee Moffitt Cancer Center

PROTOCOL WRITER I

Tampa, FL · On-site

$31.21 - $39.21/hr

With an emphasis on investigator-initiated, early phase clinical trials, the clinical research Protocol Writer works with clinical investigators to write, edit and complete clinical trial protocols ...

Moffitt Cancer Center

PROTOCOL WRITER I

Tampa, FL · On-site

With an emphasis on investigator-initiated, early phase clinical trials, the clinical research Protocol Writer works with clinical investigators to write, edit and complete clinical trial protocols ...

Moffitt Cancer Center

Protocol Writer I

Tampa, FL · On-site

With an emphasis on investigator-initiated, early phase clinical trials, the clinical research Protocol Writer works with clinical investigators to write, edit and complete clinical trial protocols ...

Eurofins

Stability Protocol Writer

Lancaster, PA · On-site

The Group also has a rapidly developing presence in highly specialised and molecular clinical ... Support continuous process improvements related to protocol writing, workflow efficiency, and ...

Aequor Technologies

Medical Writer

Princeton, NJ · On-site

Medical Writer Must have 5 -7 years of experience. POSITION SUMMARY: The Medical Writer a ... FDA and EMA) including Clinical Study Reports, Investigator Brochures, Protocols, Protocol ...

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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.
PROTOCOL WRITER I

PROTOCOL WRITER I

H. Lee Moffitt Cancer Center

Tampa, FL • On-site

$31.21 - $39.21/hr

Full-time

This job post has expired today. Applications are no longer accepted.

Moffitt Cancer Center rating

8.1

Company rating: 8.1 out of 10

Based on 92 frontline employees who took The Breakroom Quiz

72nd of 867 rated healthcare providers

Job description

Job Summary:
With an emphasis on investigator-initiated, early phase clinical trials, the clinical research Protocol Writer works with clinical investigators to write, edit and complete clinical trial protocols and related documents necessary to accurately and timely submit clinical trial projects to the Scientific Review Committee (SRC).
Works under the direction of the Principal Investigator (PI) to edit, write, and gather technical and scientific documentation required to conceptualize, prepare, and deliver complete clinical protocol proposals to the SRC.
Responsibilities also include working with the Clinical Trials Office to ensure adherence to Moffitt's standards and regulatory requirements and with the PI, working with external sponsors on study design.
Secondary responsibilities include supporting clinical science editing activities. For select grants that include clinical trials, the position will work with Grant Administrators on the clinical research portion of the proposal, including developing the protocol and related documents outlined in the PHS Human Subjects and Clinical Trials Information Form as required for NIH defined clinical trials.
Position requires deadline-driven approach and ability to handle multiple concurrent projects, each with varying deadlines for execution.
Minimum Requirements:
Bachelors Degree
Strong scientific/medical/health-related background with clinical research experience preferred. Experience must include at least 2 years of relevant medical writing industry experience and a proven track record in writing high quality regulatory documents.
Preferred:
MA, MS, MD, PharmD, or PhD with 1 years scientific experience and/or clinical research experience.

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