2

Entry Level Clinical Protocol Writer Jobs (NOW HIRING)

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 ...

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 ...

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 ...

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 ...

This position is ideal for entrylevel clinical professionals looking to join the Clinical ... Align Protocols and customer needs . This role is critical to supporting highquality clinical ...

next page

Showing results 1-20

Entry Level Clinical Protocol Writer information

See salary details

$25

$54

$83

How much do entry level clinical protocol writer jobs pay per hour?

As of Jun 7, 2026, the average hourly pay for entry level 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 most commonly searched types of Clinical Protocol Writer jobs? The most popular types of Clinical Protocol Writer jobs are:
PROTOCOL WRITER I

$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 869 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.

What Moffitt Cancer Center employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom