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Remote Clinical Research Protocol Writer Jobs (NOW HIRING)

Moffitt

PROTOCOL WRITER I

$31.99 - $48.80/hr

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 ...

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 ...

WEP Clinical

Senior Clinical Research Associate

They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential ... Excellent written and verbal communication; confident stakeholder engagement * Solid understanding ...

WEP Clinical

Senior Clinical Research Associate

They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential ... Excellent written and verbal communication; confident stakeholder engagement * Solid understanding ...

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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Remote Clinical Research Protocol Writer information

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$25

$54

$83

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

As of Sep 6, 2026, the average hourly pay for remote 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 does a remote clinical research protocol writer do?

A Remote Clinical Research Protocol Writer is responsible for creating detailed documents that outline the objectives, design, methodology, and organization of clinical research studies. They collaborate with clinical teams, researchers, and regulatory experts to ensure that protocols comply with regulatory standards and support the scientific goals of the study. Working remotely, they use digital tools to gather data, review literature, and communicate with stakeholders. Their work is essential for guiding clinical trials, ensuring participant safety, and supporting regulatory submissions.

What are the key skills and qualifications needed to thrive as a remote clinical research protocol writer?

To excel as a Remote Clinical Research Protocol Writer, you need a background in life sciences or healthcare, strong scientific writing skills, and familiarity with regulatory guidelines such as GCP and ICH. Proficiency in tools like Microsoft Office, reference management software, and electronic data capture (EDC) systems is commonly required. Exceptional attention to detail, time management, and the ability to collaborate virtually with multidisciplinary teams are vital soft skills. These competencies ensure the creation of accurate, compliant, and clear research protocols that support successful clinical trials and regulatory submissions.

How does a remote clinical research protocol writer typically collaborate with research teams and stakeholders?

As a Remote Clinical Research Protocol Writer, you will frequently collaborate with cross-functional teams such as clinical trial managers, biostatisticians, regulatory affairs specialists, and medical experts. Communication often occurs through virtual meetings, emails, and shared document platforms to ensure all protocol elements meet regulatory, ethical, and scientific standards. You may be responsible for gathering input, incorporating feedback, and ensuring that protocols are clear and aligned with study objectives. This collaborative process is essential for creating robust documents that support successful study execution and regulatory submissions.

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

AspectRemote Clinical Research Protocol WriterRemote Clinical Research Associate
CredentialsTypically requires a degree in life sciences, clinical research certification preferredRequires a degree in life sciences or related field, often with GCP or ICH certifications
Work EnvironmentPrimarily writing and editing protocols remotely, collaborating with teamsMonitoring clinical sites remotely, ensuring protocol compliance
Industry UsageUsed mainly in pharmaceutical and biotech companies for protocol developmentUsed across clinical trial sites for monitoring and data collection

The Remote Clinical Research Protocol Writer focuses on creating and editing clinical trial protocols, while the Remote Clinical Research Associate is responsible for monitoring trial sites and ensuring compliance. Both roles require knowledge of clinical research processes and often share similar certifications, but their daily tasks and work environments differ significantly.

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Remote Clinical Research Protocol Writer jobs near you
Infographic showing various Remote 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.

PROTOCOL WRITER I

Moffitt

Remote

$31.99 - $48.80/hr

Full-time

Posted 16 days ago

Job description

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer.As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times' Top Workplaces.

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.

Protocol Writer I

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:

Bachelor's 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 Qualifications:
MA, MS, MD, PharmD, or PhD with 1 year of scientific experience and/or clinical research experience.

Salary Range

$31.99 - $48.80

Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.


We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce.

Moffitt Career Site

If you have the vision, passion, and dedication to contribute to our mission,then we have a place for you!

1. Equal Employment Opportunity

Moffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence.

2. Reasonable Accommodation

Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. Moffitt endeavors to make moffitt.org/careers accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact one of the Human Resources receptionists by phone at 813-745-7899 or by email atHRReceptionists@moffitt.org. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.

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