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Clinical Study Associate Jobs in Florida (NOW HIRING)

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Clinical Research Associate II

Miami, FL

Clinical Research Associate ICON is a global healthcare intelligence and clinical research ... Contributing to the preparation and review of study documentation, including protocols and clinical ...

ICON

Clinical Research Associate II

Miami, FL · On-site +1

Clinical Research Associate ICON is a global healthcare intelligence and clinical research ... Contributing to the preparation and review of study documentation, including protocols and clinical ...

ICON plc

Clinical Research Associate II

Miami, FL

Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical ... Contributing to the preparation and review of study documentation, including protocols and clinical ...

ICON plc

Clinical Research Associate

Bell, FL · On-site

Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical ... Contributing to the preparation and review of study documentation, including protocols and clinical ...

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Clinical Research Associate

Tampa, FL

Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical ... Contributing to the preparation and review of study documentation, including protocols and clinical ...

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Clinical Research Associate

Miami, FL

Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical ... Contributing to the preparation and review of study documentation, including protocols and clinical ...

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Clinical Research Associate

Orlando, FL

Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical ... Contributing to the preparation and review of study documentation, including protocols and clinical ...

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Clinical Study Associate information

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How much do clinical study associate jobs pay per hour?

As of May 30, 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 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 Clinical Study Associates?

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 most commonly searched types of Clinical Study jobs in Florida? The most popular types of Clinical Study jobs in Florida are:
What are popular job titles related to Clinical Study Associate jobs in Florida? For Clinical Study Associate jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Clinical Study Associate jobs in Florida look for? The top searched job categories for Clinical Study Associate 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:
Clinical Study Associate jobs near you

Clinical Research Coordinator

Atlas Clinical Research

New Port Richey, FL • On-site

$21 - $22/hr

Full-time

Posted 9 days ago

Job description

  • Seeking candidates who live in or near Palm Harbor, FL only as this is an onsite position
    • Job Summary

    The Clinical Research Coordinator works closely with the Research/Sub-Investigator managing study conduct from study selection through study closeout. The Clinical Research Coordinator is responsible for the quality and integrity of their assigned clinical studies in accordance with Good Clinical Practice (GCP) and applicable regulations.

    Key Responsibilities
  • Maintain strict confidentiality in compliance with and FDA, ICH, GCP and HIPAA guidelines.
  • Organize, coordinate, and help ensure the overall integrity of assigned research trials. The Principal Investigator provides the overall direction in a clinical study, but the Clinical Research Coordinator has a significant role in the clinical study activities.
  • Identify, evaluate, and recruit study subjects for participation in clinical trials, according to protocol requirements.
  • Perform tasks delegated by the Principal Investigator, including consenting, documenting medical history, collecting and tracking vital signs and adverse events, collecting and processing specimen, administering medications, maintaining sufficient inventory of investigational product and lab kits.
  • Follow current Food and Drug Administration (FDA), International Conference on Harmonization (ICH) and Good Clinical Practices (GCP) regulations and guidelines.
  • Ensure that all patient visit procedures and activities are conducted in strict compliance with the protocol and FDA, ICH, GCP and HIPAA guidelines
  • Ensure the safety and welfare of the study subjects by providing subject care and data collection procedures in adherence with the assigned protocol and in accordance with good clinical research principles.
  • Gain a detailed understanding of assigned study protocols and conditions under study in order to properly answer questions and discuss appropriate study details with patients, investigators, coworkers, individuals in the community, and Sponsor and/or CRO representatives.
  • Recruit new study subjects for protocol participation via continuous interaction with the Investigator(s), routine review of medical records and database records, and screening of potential study subjects who respond to advertisements.
  • Screen potential study candidates prior to enrollment according to the protocol’s inclusion and exclusion criteria.
  • Obtain the study subjects' informed consent according to SOP 2C, Informed Consent Process and in compliance with 21 CFR and ICH.
  • Schedule study subjects' subsequent study visits.
  • Report all serious adverse events to the Principal Investigator, Director of Clinical Operations and Business Development, and Regulatory.
  • Keep investigators informed of the status of all current studies, participating study subjects and enrollment status.
  • Maintain adequate and accurate case histories (i.e., source documentation) for each study subject.
  • Promptly complete and maintain (electronic) case report forms for each study subject per Sponsor requirements and respond to all queries in a timely fashion.
  • Maintain accurate and complete records of the receipt, inventory, dispensing, and return of all clinical supplies (e.g. study drug, Holter monitors, electronic diaries, etc.) in strict accordance with protocol requirements.
  • Assist the Investigators as directed.
  • Communicate with the Sponsor/CRO regarding study activities as necessary.
  • Meet with the Sponsor's representatives to discuss the conduct of the study and review study data.
  • Handle and process specimens for laboratory analysis as described in the laboratory manual and the protocol and ship the specimens according to IATA Dangerous Goods and Hazardous Materials Regulations.
  • Perform additional duties and projects as assigned
    • Qualifications
  • Excellent communications skills, strong familiarity with medical terminology and medications, and the ability to understand and communicate protocol requirements to others.
  • Able to work effectively and professionally with patients, other research personnel, physicians/investigators, monitors, and others involved in the clinical study.
  • CPRcertified or is willing to become CPRcertified.
  • Able to perform the following: ECGs, phlebotomy, blood pressure, vitals, medical history evaluation.
  • Willing to travel to investigator offices and potentially sponsor conferences, and be willing to participate in health fairs.
  • Detailoriented person with the ability to collect, complete, compile, and analyze information.
  • Able to work independently and efficiently on multiple tasks, with strong time management skills.
    • Education and Experience
  • Associate or bachelor’s degree in related field
  • Medical background and knowledge
  • Experience in clinical research preferred

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