1

Clinical Study Associate Jobs in Florida (NOW HIRING)

Showing results 21-40

Clinical Study Associate information

See Florida salary details

$9

$23

$41

How much do clinical study associate jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for clinical study associate in Florida is $23.57, according to ZipRecruiter salary data. Most workers in this role earn between $15.82 and $31.06 per hour, depending on experience, location, and employer.

What is a clinical study associate?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

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

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

What are the key skills and qualifications needed to thrive as a clinical study associate, and why are they important?

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

What are some common challenges clinical study associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.
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 Associate jobs? Cities in Florida with the most Clinical Study Associate job openings:
Infographic showing various Clinical Study Associate job openings in Florida as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 17% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $49,025 per year, or $23.6 per hour.

Clinical Support Associate

Velocity Clinical Research, Inc.

Edgewater, FL • On-site

Temporary

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago


Velocity Clinical Research rating

7.3

Company rating: 7.3 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

76th of 120 rated laboratories


Job description

Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.

As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.

Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.

Summary:

The Clinical Support Associate assists the Clinical Operations Team within a limited scope of defined responsibilities in carrying out one of the assigned roles (collection/processing of laboratory samples, data entry of clinical data or administrative/front office support).


Duties/Responsibilities:

  • Phlebotomy/Laboratory Responsibilities:
    • Assist in the conduct of clinical trials by performing phlebotomy and laboratory tasks in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs
    • Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations
    • Process, package and ship laboratory specimens as required per protocol and IATA regulations, if applicable
    • Track, order and maintain inventory of all laboratory and study related supplies throughout course of the clinical trial
    • Communicate with coworkers, leadership, study subjects, sponsors, CROs, and vendors under the direction of the Clinical Research Team
    • Maintain confidentiality of patient protected health information
    • Escalate potential patient safety issues to Clinical Research Team
    • Clean, organize, and disinfect the patient care, lab and lab equipment areas as needed
  • Data Entry Responsibilities:
    • Assist in the conduct of clinical trials by performing data entry tasks in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs under the direction of the Clinical Research Team
    • Enter source data into the sponsor's and/or vendor’s data portal
    • Resolve basic queries that do not require a change in the clinical source chart per Velocity SOPs
    • Escalate missing and/or inconsistent data identified in the subject’s chart to Clinical Research Team
    • Demonstrate basic understanding of good documentation practices when transferring data to sponsor/CRO data capture systems
    • Maintain confidentiality of patient protected health information
  • Front Office/Admin Core:
    • Maintain confidentiality of patient protected health information
    • Prepare source document charts, copy and/or file medical records and study related documents as required
    • Perform front office duties as needed including but not limited to answering phones, scheduling subjects appointments, making reminder calls and updating patient tracking systems
    • Instruct patients on completing applicable paperwork upon check in
    • Other duties as assigned

Education/Experience:

  • High school graduate and/or technical degree

Required Licenses/Certifications:

  • Phlebotomy if applicable and required by state law

Required Skills:

  • Basic knowledge of medical terminology
  • Basic ability to use the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.
  • Basic understanding of verbal, written, and organizational skills
  • Ability to work as a team player
  • Ability to read, write, and speak English
  • Ability to multi-task
  • Ability to follow written guidelines
  • Ability to be flexible/adapt as daily schedule may change rapidly

Required Physical Abilities:

  • Sit or stand for long periods of time
  • Communicate in person and by a telephone
  • Limited walking required
  • Limited to lifting up to 30 pounds

NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required.  Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change.  All employees are expected to perform their duties within their ability as required by the job and/or as requested by management.



What Velocity Clinical Research employees say

Hours and flexibility

Workplace

Get the full story on Breakroom