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Clinical Programmer Jobs in Miami, FL (NOW HIRING)

Abbott

Principal Clinical Specialist

Miami, FL · On-site

Provides engineering, sales, education and clinical support in response to the most complex field inquiries on a 24-hour, on-call basis. Demonstrates a thorough command of all EP products, related ...

Abbott

Principal Clinical Specialist

Miami, FL · On-site

Provides engineering, sales, education and clinical support in response to the most complex field inquiries on a 24-hour, on-call basis. Demonstrates a thorough command of all EP products, related ...

Abbott

Principal Clinical Specialist

Miami, FL

Provides engineering, sales, education and clinical support in response to the most complex field inquiries on a 24-hour, on-call basis. Demonstrates a thorough command of all EP products, related ...

Saluda Medical

Clinical Specialist - Miami, FL

Miami, FL · On-site

$90 - $130/hr

Serve as primary resource for clinical support including, but not limited to: troubleshooting, programming, and patient follow-up for company products. * Perform patient follow-up to assure customer ...

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All JobsClinical Programmer JobsClinical Programmer Jobs in Miami, FL

Clinical Programmer information

See Miami, FL salary details

$23

$61

$98

How much do clinical programmer jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for clinical programmer in Miami, FL is $61.85, according to ZipRecruiter salary data. Most workers in this role earn between $51.20 and $70.00 per hour, depending on experience, location, and employer.

What is a clinical programmer?

Clinical programmers are professionals who design, develop, and maintain computer programs used to manage and analyze clinical trial data in the pharmaceutical and biotech industries. They work closely with data managers, statisticians, and clinical teams to ensure data accuracy and regulatory compliance. Their responsibilities often include writing programs for data cleaning, statistical analysis, and generating reports using tools like SAS or R. Clinical programmers play a key role in ensuring that clinical trial data is processed efficiently and meets industry standards.

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

To thrive as a Clinical Programmer, you need strong proficiency in programming languages like SAS or R, a solid understanding of clinical trial processes, and typically a degree in life sciences, computer science, or a related field. Expertise with clinical data management systems (CDMS), electronic data capture (EDC) tools, and CDISC standards such as SDTM and ADaM is often required. Attention to detail, problem-solving ability, and effective communication are vital soft skills for ensuring data accuracy and collaborating with cross-functional teams. Mastery of these skills ensures the integrity and reliability of clinical trial data, supporting regulatory compliance and successful study outcomes.

How does a clinical programmer typically collaborate with biostatisticians and data managers during a clinical trial?

Clinical Programmers work closely with biostatisticians and data managers throughout the clinical trial process. They are responsible for programming data listings, tables, and figures based on statistical analysis plans provided by biostatisticians. Collaboration involves ensuring data integrity, resolving data discrepancies, and implementing database validation checks, often through regular meetings and shared documentation. This teamwork is essential for maintaining data quality and meeting regulatory requirements, making strong communication and coordination skills important in the role.

What is the difference between Clinical Programmer vs Data Manager?

AspectClinical ProgrammerData Manager
Required CredentialsBachelor's degree in life sciences, computer science, or related field; programming skills in SAS, R, or SQLBachelor's degree in health sciences, statistics, or related field; experience with data management software
Work EnvironmentCollaborates with statisticians, data managers, and clinical teams to develop and validate data reportsOversees data collection, validation, and database management for clinical trials
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, clinical research organizations

While both Clinical Programmers and Data Managers work within clinical research, Clinical Programmers primarily focus on developing data reports and programming analysis datasets, whereas Data Managers handle data collection, validation, and database management. Both roles require strong analytical skills and familiarity with clinical data standards, often working closely together to ensure data quality and integrity in clinical trials.

What are popular job titles related to Clinical Programmer jobs in Miami, FL?

For Clinical Programmer jobs in Miami, FL, the most frequently searched job titles are:

What job categories do people searching Clinical Programmer jobs in Miami, FL look for?

The top searched job categories for Clinical Programmer jobs in Miami, FL are:

Clinical Programmer jobs near you
Infographic showing various Clinical Programmer job openings in Miami, FL as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $128,656 per year, or $61.9 per hour.

Clinical Engineer System Integration II

Miami Children's Hospital

Miami, FL • On-site

$75 - $95/hr

Other

Posted 3 days ago

New

Job description

Clinical Engineer System Integration II (301472)

Acts as technical subject matter expert on medical device connectivity and provides expert knowledge in developing and maintaining interfaces in a healthcare environment. Ensures effective and safe procurement, deployment, and sustainment of integrated medical devices/systems. Serves as a medical device/system subject matter expert to clinical staff, vendors, and the Clinical Engineering department. Supports, among others, the following integrated medical devices/systems: patient monitoring, nurse call, infusion pumps, vital signs, EEG, perfusion systems, OR video integration, cardiology ultrasounds, interactive patient systems, environmental monitoring systems, DICOM nodes, post‑processing software, gastrointestinal systems, digital dental systems and review/acquisition software, HL7 brokers, Cerner EMR, and CMMS. Oversees multiple medical device/system projects with diverse stakeholders, timelines, and resources. Sustains medical device/system hardware, software, firmware, networking, servers, clients, databases, and interfaces with the support of clinical staff, in‑house technical resources, and vendors. Sustainment scenarios include resolving end‑user issues, supporting downtimes, requesting feature requests, performing vendor remediation, and responding to recalls or patient incident investigations.

Job Specific Duties
  • Serves as a medical device/system subject matter expert to clinical staff, vendors, and the Clinical Engineering department.
  • Responsible for the assessment, design, procurement, installation, monitoring, maintenance, troubleshooting, documentation, configuration, performance, and testing of medical device/system hardware, software, firmware, networking, servers, clients, databases, and interfaces with the support of clinical staff, in‑house technical resources, and vendors.
  • Responsible for resolving end‑user issues, supporting downtimes, requesting feature requests, performing vendor remediation, and responding to recalls or patient incident investigations.
  • Develops and maintains an up‑to‑date inventory and technical reference documentation of medical devices/systems and their interconnections for use in end‑user issues, downtimes, feature requests, vendor remediation, recalls, repairs, upgrades, incident investigations, or capital planning.
  • Oversees and participates in multiple medical device/system projects with diverse stakeholders, timelines, and resources.
  • Monitors and adopts the industry's and health system's latest best practices for integrated medical devices/systems, specifically for risk assessments, IT change management, FDA or vendor hazard/recalls, or patient incident root cause analysis.
  • Juggles multiple medical device/system issues requiring adequate response, delegation, prioritization, or escalation.
  • Participates in a rotating on‑call schedule to respond to medical device/system end‑user issues and device/system downtimes in a 24/7/365 environment.
  • Provides functional and technical guidance to assigned personnel on a daily basis including scheduling, monitoring, reviewing of systems studies, project and program.
Qualifications
  • Bachelor's Degree in Biomedical Engineering or related major (OR) 5+ years of equivalent relevant experience.
  • 4-7 years of hands‑on experience in medical systems configuration and administration.
  • 4-7 years of experience designing, implementing, and supporting clinical application systems.
  • 4-7 years of work experience with SQL Server relational database systems.
  • 4-7 years of work experience in HL7 interface engines.
Knowledge, Skills, and Abilities
  • Healthcare Technology Management and Information Technology relevant certifications strongly preferred.
  • Ability to communicate effectively both verbally and writing.
  • Strong working knowledge of healthcare technology management, project management, information technology, and process improvement.
  • Strong working knowledge of Windows OS, MAC OS, Linux OS, HL7 brokers, XML, JAVA, SQL, DICOM, and Cerner EMR.
  • Strong working knowledge of patient monitoring, nurse call, infusion pumps, vital signs, EEG, perfusion, OR/Cath Lab video integration, Cardiology device/systems, interactive patient systems, environmental monitoring systems, DICOM nodes, post processing software, gastrointestinal systems, dental systems, HL7 brokers, and CMMS.
  • Strong soft skills (communication, flexibility, leadership, teamwork, time management, creativity, ability to work under pressure, self‑motivation, accountability, etc.)
  • Practical experience with project delivery and systems development.
  • Experience in leading hospital applications suites preferred.
  • Working knowledge of HL7 standards and custom interface products.
  • Strong understanding of enterprise Wide Area Network (WAN), Local Area Network (LAN), TCP/IP, Ethernet.
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