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Clinical Research Study Assistant Jobs in Florida

Actalent

Clinical Research Supervisor

Orlando, FL

$90K - $115K/yr

Function as a clinical study coordinator and assist in mentoring clinical study coordinators and research staff. * Work closely with Core Managers to schedule clinical operations and facilitate the ...

Panoramic Health

Clinical Research Team Lead

Tampa, FL · On-site

The Team Lead will provide site-level leadership, serving as a resource, mentor, and preceptor for Clinical Research Coordinators and Research Assistants while maintaining an active role in study ...

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All JobsClinical Research Study JobsClinical Research Study Assistant JobsClinical Research Study Assistant Jobs in Florida

Clinical Research Study Assistant information

See Florida salary details

$6

$16

$34

How much do clinical research study assistant jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical research study assistant in Florida is $16.97, according to ZipRecruiter salary data. Most workers in this role earn between $12.93 and $19.42 per hour, depending on experience, location, and employer.

What does a clinical research study assistant do?

A Clinical Research Study Assistant supports the daily operations of clinical trials and research studies. Their tasks typically include preparing study materials, collecting and entering data, scheduling and coordinating participant visits, and ensuring that study protocols are followed. They may also assist with regulatory documentation and serve as a point of contact for study participants. This role is essential in helping research teams maintain accurate records and comply with ethical and legal standards. Clinical Research Study Assistants often work under the supervision of study coordinators or principal investigators.

What skills and qualifications are needed to be a clinical research study assistant?

To thrive as a Clinical Research Study Assistant, you need a solid understanding of clinical research protocols, data collection, and regulatory compliance, often supported by a bachelor’s degree in a life science or related field. Familiarity with electronic data capture systems (EDC), Microsoft Office Suite, and Good Clinical Practice (GCP) certification is highly beneficial. Strong organizational skills, attention to detail, and effective communication set standout candidates apart. These skills are crucial for maintaining study integrity, ensuring accurate data, and supporting smooth collaboration across research teams.

How does a clinical research study assistant collaborate with other members of the research team?

A Clinical Research Study Assistant works closely with principal investigators, study coordinators, and other research staff to ensure the smooth operation of clinical trials. Collaboration often involves coordinating participant scheduling, communicating protocol updates, and assisting with data collection and entry. These professionals also help ensure regulatory compliance by working with regulatory specialists and contribute to team meetings where study progress and challenges are discussed. Strong teamwork and communication skills are essential for successfully supporting the study's goals and maintaining high-quality research standards.

What is the difference between Clinical Research Study Assistant vs Clinical Research Coordinator?

AspectClinical Research Study AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree or relevant certificationRequires a bachelor's degree, often with additional certifications or experience
Work EnvironmentAssists in data collection, documentation, and administrative tasks in clinical settingsManages study protocols, patient recruitment, and regulatory compliance in clinical trials
Employer & Industry UsageUsed by research institutions, hospitals, and pharmaceutical companiesCommonly employed in similar settings, often overseeing study operations

The Clinical Research Study Assistant primarily supports data collection and administrative tasks, while the Clinical Research Coordinator manages study protocols and patient interactions. Both roles are essential in clinical trials, with the coordinator typically having more responsibilities and requiring additional experience or certifications.

Is a Clinical Research Study Assistant a good career?

A Clinical Research Study Assistant is a valuable entry-level role in clinical research, supporting study coordination, data collection, and regulatory compliance. It offers opportunities to gain experience in the healthcare and pharmaceutical industries, with potential advancement into more specialized or supervisory positions. The role typically requires attention to detail, organizational skills, and familiarity with clinical trial protocols.

What are the most commonly searched types of Clinical Research Study jobs in Florida?

The most popular types of Clinical Research Study jobs in Florida are:

What cities in Florida are hiring for Clinical Research Study Assistant jobs?

Cities in Florida with the most Clinical Research Study Assistant job openings:

Clinical Research Study Assistant jobs near you
Infographic showing various Clinical Research Study Assistant job openings in Florida as of August 2026, with employment types broken down into 2% As Needed, 77% Full Time, 15% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $35,302 per year, or $17 per hour.

Clinical Research Assistant / Recruiter

Metabolic Research Institute Inc.

West Palm Beach, FL • On-site

$22 - $24/hr

Full-time

Medical, Dental, Vision, Life, PTO

Re-posted 14 days ago

Job description

Job description

Metabolic Research Institute is looking for a Full Time Clinical Research Assistant / Recruiter for busy Clinical Research Center in West Palm Beach, FL.

IDEAL CANDIDATES:

Research Assistant / Medical Assistant Experience

Recruitment Experience

Medical Terminology

Knowledge of Diabetes

Requirements:

MUST have at least 2 years of experience as an assistant to be considered for this role.

  • Must be detail oriented.
  • Must have exceptional organizational skills.
  • Recruitment experience.
  • Must be able to multitask.
  • Front Desk experience and patients interaction.
  • Computer knowledge of EDC.
  • Computer knowledge of Microsoft Office
  • Previous research experience required.
  • Bilingual in Spanish is a plus
  • Successful candidate should have the ability to work independently.
  • Must have a professional speaking manner and appearance.
We offer competitive salary and benefits.
About the company:

Metabolic Research Institute, Inc. (“MRI”), is a private Clinical Research Company located in West Palm Beach, FL, dedicated to the advancement of science and improvement of quality of life by providing clinical research study services to pharmaceutical sponsors and medical device manufacturers.
By acting as an intermediary for the pharmaceutical and biotech community to access qualified subjects, we are able to provide the opportunity to explore promising new therapies while granting access to these experimental therapies to the people who need them. We are committed to an ethical, innovative, caring and professional environment for our sponsors, investigative team, and study participants.
Our mission at the Metabolic Research Institute is to provide our patients and sponsors with the highest quality of clinical research available in today’s medical professional environment. We are committed to delivering efficient and timely research data, while focusing on strict adherence to protocol guidelines.
Benefit Conditions:
  • Only full-time employees eligible
This Company Describes Its Culture as:
  • Detail-oriented -- quality and precision-focused
  • Team-oriented -- cooperative and collaborative
Job Type: Full-time
Pay: $22.00 - $24.00 per hour
Expected hours: 40 per week
Benefits:
  • Dental insurance
  • Health insurance
  • Life insurance
  • Paid time off
  • Vision insurance
Schedule:
  • 8 hour shift
Education:
  • High school or equivalent (minimum)
Experience:
  • Clinical Trials: 2 years (Required)
  • Clinical Research: 2 years (Required)
Work Location: In person