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Clinical Study Assistant Jobs in Florida (NOW HIRING)

Oneoncology

Medical Assistant

Aventura, FL · On-site

$17.25 - $22/hr

Performs administrative and clinical duties under the direction of the Physician or Physician ... Schedule and follow-up on all diagnostic studies that are ordered including proper documentation ...

Oneoncology

Medical Assistant

Pembroke Pines, FL · On-site

$16.50 - $21/hr

Performs administrative and clinical duties under the direction of the Physician or Physician ... Schedule and follow-up on all diagnostic studies that are ordered including proper documentation ...

Oneoncology

Medical Assistant

Aventura, FL · On-site

$17.25 - $22/hr

Performs administrative and clinical duties under the direction of the Physician or Physician ... Schedule and follow-up on all diagnostic studies that are ordered including proper documentation ...

Oneoncology

Medical Assistant

Pembroke Pines, FL

$16.50 - $21/hr

Performs administrative and clinical duties under the direction of the Physician or Physician ... Schedule and follow-up on all diagnostic studies that are ordered including proper documentation ...

SunState Medical Specialists

Medical Assistant

Aventura, FL · On-site

$17.25 - $22/hr

Performs administrative and clinical duties under the direction of the Physician or Physician ... Schedule and follow-up on all diagnostic studies that are ordered including proper documentation ...

SunState Medical Specialists

Medical Assistant

Aventura, FL · On-site

$17.25 - $22/hr

Performs administrative and clinical duties under the direction of the Physician or Physician ... Schedule and follow-up on all diagnostic studies that are ordered including proper documentation ...

SunState Medical Specialists

Medical Assistant

Miami, FL · On-site

$17 - $21.75/hr

Performs administrative and clinical duties under the direction of the Physician or Physician ... Schedule and follow-up on all diagnostic studies that are ordered including proper documentation ...

Oneoncology

Medical Assistant

Miami, FL · On-site

$17 - $21.75/hr

Performs administrative and clinical duties under the direction of the Physician or Physician ... Schedule and follow-up on all diagnostic studies that are ordered including proper documentation ...

Oneoncology

Medical Assistant

Crestview, FL · On-site

$15 - $19.25/hr

Performs administrative and clinical duties under the direction of the Physician or Physician ... Schedule and follow-up on all diagnostic studies that are ordered including proper documentation ...

Oneoncology

Medical Assistant

Boca Raton, FL · On-site

$16.75 - $21.50/hr

Performs administrative and clinical duties under the direction of the Physician or Physician ... Schedule and follow-up on all diagnostic studies that are ordered including proper documentation ...

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

Clinical Study Assistant information

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$8

$15

$21

How much do clinical study assistant jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical study assistant in Florida is $15.12, according to ZipRecruiter salary data. Most workers in this role earn between $12.40 and $17.40 per hour, depending on experience, location, and employer.

What is a clinical study assistant?

Clinical Study Assistants are professionals who support the conduct of clinical trials by handling administrative tasks, maintaining study documentation, and ensuring regulatory compliance. They work closely with clinical research teams to coordinate schedules, communicate with study sites, and help manage trial materials. Their role is crucial in ensuring that clinical studies run smoothly, efficiently, and according to protocols and regulatory guidelines.

What are the key skills and qualifications needed to thrive as a clinical study assistant?

To thrive as a Clinical Study Assistant, you need strong organizational skills, attention to detail, and a background in life sciences or related fields, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory documentation processes is typically required. Effective communication, teamwork, and problem-solving skills help you navigate complex study protocols and collaborate with diverse stakeholders. These abilities are crucial for ensuring the accuracy, compliance, and smooth operation of clinical research studies.

What are the main challenges a clinical study assistant might face when supporting clinical trial operations?

A Clinical Study Assistant often encounters challenges such as managing multiple tasks under tight deadlines, ensuring accurate documentation, and coordinating communication between research teams, sponsors, and regulatory bodies. Additionally, adapting to evolving study protocols and maintaining compliance with strict regulatory requirements can be demanding. Strong organizational skills, attention to detail, and proactive communication are essential for navigating these challenges successfully.

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

AspectClinical Study AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldUsually requires a bachelor's degree, often with additional certifications in clinical research
Work EnvironmentSupports clinical trials in hospitals, research centers, or pharmaceutical companiesManages entire clinical studies, coordinating between sites, staff, and sponsors
Employer & IndustryHospitals, research institutions, pharmaceutical companiesAcademic medical centers, hospitals, research organizations
Search & Comparison IntentOften compared for entry-level roles supporting clinical trialsCompared for roles with broader responsibilities in clinical study management

The Clinical Study Assistant primarily supports clinical trial activities by assisting with data collection and documentation, while the Clinical Research Coordinator manages the overall conduct of the study, including patient recruitment and compliance. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.

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

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

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

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

Clinical Study Assistant jobs near you
Infographic showing various Clinical 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 $31,446 per year, or $15.1 per hour.

CLINICAL RESEARCH COORDINATOR III

University of Alabama at Birmingham

Tampa, FL • On-site

$60.83 - $98.86/hr

Other

Posted 2 days ago

New

University Of Alabama At Birmingham rating

7.7

Company rating: 7.7 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

264th of 628 rated colleges and universities

Job description

Job Description – CLINICAL RESEARCH COORDINATOR III (T236091)

The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center, is seeking a Clinical Research Coordinator III.

General Responsibilities

Serve as a lead coordinator by providing oversight to less experienced staff to ensure quality and regulatory compliance with clinical research operations.

Coordinate and manage the research study lifecycle from start‑up through close‑out.

Conduct all applicable clinical and administrative activities required by the protocol such as screening, scheduling, consenting, assessing, ordering, collecting, documenting and shipping under the auspices of Good Clinical Practice (GCP).

Key Duties & Responsibilities
  • Lead protocol screening and participant eligibility determination, working alongside other team members to ensure compliance.
  • Oversee CRC I/II and CRNC I/II in review of study start‑up, SIV planning, subject management, data query resolution, and source document development.
  • Conduct all study activities in accordance with the protocol, IRB regulations, and GCP.
  • Provide quality patient care to patients and their families within the area of clinical specialty.
  • Manage the life cycle of the clinical trial from study start‑up through trial maintenance to study closure.
  • Coordinate and organize patient care, including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
  • Perform the informed consent process following GCP.
  • Communicate effectively with CRC and CRNC regarding lab reports and adverse events to ensure protocol compliance with dosing.
  • In conjunction with the PI or Director, interpret and apply current research findings in the area of clinical specialty and report findings in professional journals and local, state, and national conferences.
  • Schedule and coordinate patient visits and procedures, and track the study participant calendar per the protocol schedule of events.
  • Coordinate patient care and/or patient follow‑up functions of the clinical study, including planning and developing related activities.
  • Arrange access to study medications, including authorization for prescriptions.
  • Employ strategies to maintain recruitment and retention rates.
  • In collaboration with the CTO regulatory team and coordinators, complete and submit Adverse Event (AE) and Serious Adverse Event (SAE) reports in a timely manner and in compliance with FDA, sponsor, and institutional policies.
  • Complete OnCore worksheet to ensure proper protocol billing.
  • Perform other duties as assigned.
Annual Salary Range

$60,835 - $98,855

Qualifications

Bachelor’s degree in a related field and five (5) years of related experience required. Work experience may NOT substitute for education requirement. Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification preferred.

Preferences
  • Clinical research experience.
  • Ability to lead others in the coordination of research activities involved in conducting oncology clinical trials.
  • Knowledge of clinical research regulatory/compliance affairs.
  • Working knowledge of related scientific and clinical terminology.
  • Problem‑solving skills.
  • Prioritization skills.
  • Organizational skills.
  • Written and verbal communication skills.
  • Ability to walk minimally one mile a day and lift 5–10 pounds daily.
Equal Opportunity Statement

UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran’s status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB’s Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.

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About University of Alabama at Birmingham

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The University of Alabama at Birmingham is the heartbeat of Birmingham and an integral medical leader in the Southeast. The Birmingham campus is within walking distance of some of the best parks, entertainment, and dining in the region. UAB's three regional campuses expand their academic reach and responsibilities in addition to educating physicians in rural and underserved areas of the state. UAB is experiencing major and sustained investment and growth, due both to its exceptional research faculty and its culture of collaboration. Through concerted and strategic investments in its clinical and research enterprise, UAB has undergone an amazing transformation in the past five years and has strengthened its status and reputation as a leader in medical training, biomedical discovery, innovation, and patient care.

Industry

Colleges, universities, and professional schools

Company size

10,000+ Employees

Headquarters location

Birmingham, AL, US

Year founded

1859

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