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Full Time Clinical Research Protocol Writer Jobs

... 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 ...

Clinical Research Coordinator 3

Miami, FL

$23.25 - $30.75/hr

... Full Time Clinical Research Coordinator 3 to work at the UHealth Medical Campus. The Clinical ... Coordinates the implementation of multiple complex clinical research protocols. * Develops SOPs and ...

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Full Time Clinical Research Protocol Writer information

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$25

$54

$83

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

As of Aug 16, 2026, the average hourly pay for full time 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 is the difference between Full Time Clinical Research Protocol Writer vs Clinical Research Associate?

AspectFull Time Clinical Research Protocol WriterClinical Research Associate
Primary RoleDevelops and writes clinical trial protocolsMonitors and manages trial sites and data collection
Required SkillsScientific writing, regulatory knowledge, attention to detailSite management, communication, data oversight
Work EnvironmentOffice-based, collaborative with research teamsOn-site at clinical trial locations or remotely
Industry UsageUsed across pharmaceutical, biotech, and CROs for protocol developmentUsed in clinical trial sites and sponsor organizations for trial oversight

While both roles are essential in clinical research, the Full Time Clinical Research Protocol Writer focuses on creating detailed trial protocols, whereas the Clinical Research Associate oversees trial conduct and site compliance. They collaborate closely but have distinct responsibilities within the clinical research process.

What cities are hiring for Full Time Clinical Research Protocol Writer jobs?

Cities with the most Full Time 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 Full Time Clinical Research Protocol Writer jobs?

States with the most job openings for Full Time Clinical Research Protocol Writer jobs include:

Clinical Research Coordinator 1 - Multiple Myeloma

University of Miami

Miami, FL

$23.25 - $30.75/hr

Full-time

Medical, Dental

Re-posted 20 days ago


University Of Miami rating

7.7

Company rating: 7.7 out of 10

Based on 52 frontline employees who took The Breakroom Quiz

260th of 618 rated colleges and universities


Job description

Current Employees:

If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position, please review this tip sheet.

The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full-Time Clinical Research Coordinator 1to work at the UHealth campus in Miami, Fl.

CORE JOB SUMMARY
The Clinical Research Coordinator 1 serves as an entry-level clinical research professional that has a foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols. The incumbent is responsible for simple clinical research protocols and timelines.
CORE JOB FUNCTIONS
1. Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols. Maintains enrollment procedures according to the protocol.
2. Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, and project evaluation.
3. Performs moderate to complex research tests/ experiments and adapts procedures for quality improvement under supervision.
4. Understands and follows technical instructions for operating clinical research equipment, problem solves when operational failures occur.
5. Assists in observing and informing the PI/supervisor of adverse events, including those reported by study participants.
6. Addresses adverse events per protocol, advocating for study participants and quality standards throughout the lifespan of the study.
7. Identifies, reports, and helps problem solve protocol deviations and unanticipated occurrences.
8. Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
9. Knows the contents and maintenance of study-specific clinical research regulatory binders.
10. Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
11. Adheres to University and unit-level policies and procedures and safeguards University assets.
This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.
CORE QUALIFICATIONS
Education: Bachelor's degree in relevant field required
Experience: Minimum 1 year of relevant experience required
Knowledge, Skills and Abilities:

  • Learning Agility: Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands.
  • Teamwork: Ability to work collaboratively with others and contribute to a team environment.
  • Technical Proficiency: Skilled in using office software, technology, and relevant computer applications.
  • Communication: Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders.

The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.

UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for.

The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.

Job Status:

Full time

Employee Type:

Staff

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About University of Miami

Sourced by ZipRecruiter

The University of Miami, located in the beautiful Coral Gables, Florida, is a comprehensive, private research institution in the United States. Operating within the higher education industry, the institution offers a multitude of degree programs spanning over 180 majors and program through its 12 colleges. The University was founded in 1925 with the mission to disseminate knowledge, transform lives, and change the world - a mission it has held faithfully to this day. Notably, the University of Miami has gained global recognition for its commitment to research and innovation, with over $324 million in research and sponsored project funding awarded annually.

Industry

Colleges, universities, and professional schools

Company size

10,000+ Employees

Headquarters location

Coral Gables, FL, US

Year founded

1925