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Clinical Research Informatics Jobs in Florida (NOW HIRING)

... research. At Mount Sinai, we take pride in our achievements, aiming to be a beacon of quality ... Informatics Analyst, Epic Certified and Clinical experience. Job Summary The Clinical Information ...

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Clinical Research Informatics information

See Florida salary details

$38.9K

$77.4K

$122.6K

How much do clinical research informatics jobs pay per year?

As of Jul 28, 2026, the average yearly pay for clinical research informatics in Florida is $77,417.00, according to ZipRecruiter salary data. Most workers in this role earn between $56,000.00 and $86,300.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Clinical Research Informatics position, and why are they important?

Excelling in Clinical Research Informatics requires a solid background in clinical research methodologies, health informatics, data management, and often a relevant degree such as in biomedical informatics or computer science. Proficiency with data analysis tools (like SAS, R, or Python), electronic data capture systems (such as REDCap), and knowledge of healthcare regulatory standards (HIPAA, GCP) are typically expected. Strong communication, analytical thinking, and the ability to collaborate across multidisciplinary teams are important soft skills. These competencies ensure effective collection, management, and interpretation of clinical data, supporting high-quality research outcomes and regulatory compliance.

What is a Clinical Research Informatics job?

A Clinical Research Informatics job involves managing and analyzing healthcare data to support clinical research and improve patient outcomes. Professionals in this field develop and maintain databases, ensure data integrity, and utilize informatics tools to streamline clinical trials. They collaborate with researchers, clinicians, and IT specialists to optimize data collection, integration, and analysis. This role requires knowledge of biomedical research, data science, and regulatory compliance.

What are the typical daily responsibilities for someone working in Clinical Research Informatics?

Professionals in Clinical Research Informatics are usually responsible for designing and managing databases for clinical studies, ensuring data integrity, and analyzing research data to support scientific findings. They often coordinate with clinical researchers, IT specialists, and regulatory teams to develop data collection protocols and maintain compliance with industry standards. Regular tasks may include troubleshooting data issues, preparing reports, and training staff on informatics systems. This role often involves both independent work and close collaboration with multidisciplinary teams, offering a dynamic and impactful work environment.

What are the most commonly searched types of Clinical Research Informatics jobs in Florida? The most popular types of Clinical Research Informatics jobs in Florida are:
Infographic showing various Clinical Research Informatics job openings in Florida as of July 2026, with employment types broken down into 2% As Needed, 74% Full Time, 18% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $77,417 per year, or $37.2 per hour.
Clinical Research Analyst III - Clinical Research Hub

Clinical Research Analyst III - Clinical Research Hub

University of Florida

Gainesville, FL • On-site

$75K - $85K/yr

Full-time

Posted 16 days ago


University Of Florida rating

7.2

Company rating: 7.2 out of 10

Based on 108 frontline employees who took The Breakroom Quiz

384th of 612 rated colleges and universities


Job description

Clinical Research Analyst III - Clinical Research Hub
Job no: 540534
Work type: Staff Full-Time
Location: Main Campus (Gainesville, FL)
Categories: Health Care Administration/Support
Department:29011701 - MD-OR CLINICAL RESEARCH HUB
Classification Title:
Clinical Research Analyst III
Classification Minimum Requirements:
Bachelor's degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience.
Job Description:
The University of Florida Clinical Research Hub is seeking an experienced OnCore Systems Administrator / Clinical Research Team Lead to support and enhance clinical research operations through the configuration, administration, maintenance, and optimization of the OnCore Clinical Trials Management System (CTMS). In this key leadership role, you will ensure system integrity, regulatory compliance, and alignment with institutional workflows while serving as the team lead and direct supervisor for an assigned Clinical Research Analyst II (CRA II).
Working collaboratively with clinical research staff, finance, and IT teams, you will manage protocol builds, billing compliance, reporting, system integrations (including Epic), and workload coordination for your assigned team member. As the OnCore subject matter expert, you will provide training, supervision, user support, and process improvement leadership to enhance system utilization, operational consistency, and the successful execution of clinical research across the institution
More about this position:
OnCore System Administration and Team Lead Oversight
  • Configure and maintain OnCore CTMS, including user roles, permissions, system dictionaries, protocol configuration, and system upgrades.
  • Monitor system performance, troubleshoot issues, and serve as the team lead for day-to-day OnCore administration activities.
  • Assign, prioritize, and review work performed by the assigned CRA II direct report to ensure accurate, timely, and compliant completion of CTMS-related tasks.

Protocol & Calendar Build Support
  • Build and maintain study calendars, coverage analyses, and protocol records.
  • Collaborate with study teams to ensure accurate study setup and compliance with billing and regulatory requirements.
  • Provide direct guidance, quality review, and escalation support to the CRA II direct report on protocol build activities, calendar maintenance, and related workflow questions.

Data Integrity, Reporting, and Quality Review
  • Ensure data accuracy and completeness within OnCore.
  • Develop and maintain reports, dashboards, and data extracts for operational, financial, and compliance tracking.
  • Conduct audits and quality assurance checks, including review of work completed by the CRA II direct report, and implement corrective action or additional training when needed.

Training, User Support, and Staff Supervision
  • Provide onboarding, training, and ongoing support to OnCore users.
  • Develop SOPs, user guides, and training materials.
  • Serve as a subject matter expert for system-related inquiries.
  • Provide direct supervision to the assigned CRA II, including work direction, coaching, performance feedback, and support for professional development in coordination with departmental leadership.

System Integration and Process Improvement
  • Support integrations with EPIC and other institutional systems.
  • Identify workflow improvements, participate in system upgrades, and implement enhancements to optimize system use.
  • Lead process improvement efforts involving OnCore workflows and coordinate implementation activities with the CRA II direct report and other stakeholders.

Expected Salary:
$75,000 - $85,000 annually
Required Qualifications:
Bachelor's degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience.
Preferred:
The ideal candidate will possess:
  • Bachelor's degree in information systems, health informatics, clinical research, or related field; or equivalent combination of education and experience
  • Minimum of three (3) years of experience in clinical research operations, CTMS administration, or healthcare IT systems
  • Experience with clinical trial workflows and regulatory requirements (FDA, NIH, GCP)
  • Direct experience administering OnCore CTMS
  • Experience with OnCore calendar builds and coverage analysis
  • Familiarity with EPIC research billing integration
  • Experience with reporting tools (SQL, Power BI, Tableau)
  • CCRP, CCRC, or equivalent clinical research certification
  • Experience in an academic medical center or large research institution
  • Experience serving as a team lead, supervisor, or work lead in a clinical research, CTMS, or healthcare operations setting
  • Experience training, coaching, assigning work, and reviewing deliverables for clinical research staff or analysts

Special Instructions to Applicants:
Applicants must upload a copy of the following documents to be considered for this position:
Cover Letter or Letter of Interest
Curriculum Vitae or Resume
List of Three Professional References
Application must be submitted by 11:55 p.m. (ET) of the posting end date.
Health Assessment Required:No
Advertised: 13 Jul 2026 Eastern Daylight Time
Applications close: 27 Jul 2026 Eastern Daylight Time
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About University of Florida

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The University of Florida is one of the top ranked public universities in the United States (ranked top 5 amongst public universities in 2023 US news and world report). It is one of only a few comprehensive universities, having medical, veterinary, dental, nursing, public health, and engineering disciplines all co-localized on the same, contiguous campus to facilitate interdisciplinary collaboration. Gainesville is located in the northern region of Florida, within 1-1.5 hours of each coast, and just 1.5-2 hours to Orlando and Tampa. It is a small to medium-sized city with a low cost of living, excellent public and private schools, and southern hospitality. While Gainesville is widely recognized as the home of the Gators, it is quickly becoming known as a center for innovation and a place with a lifestyle that's comfortable for families, yet attractive for young professionals.

Industry

Colleges, universities, and professional schools

Company size

5,001 - 10,000 Employees

Headquarters location

Gainesville, FL, US

Year founded

1853