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Full Time Clinical Research Informatics Jobs in Florida

University of Miami

Clinical Research Coordinator 1

Miami, FL · On-site

$23.25 - $30.75/hr

The Clinical Translational Research Site is currently seeking a full-time Clinical Research Coordinator 1 to work in Miami. The Clinical Research Coordinator 1 serves as an entry level clinical ...

University of Miami

Clinical Research Coordinator 1

Miami, FL · On-site

$23.25 - $30.75/hr

The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full-Time Clinical Research Coordinator 1 to work at the UHealth campus in Miami, Fl. CORE SUMMARY The Clinical ...

University of Miami

Clinical Research Coordinator 1

Miami, FL · On-site

$23.25 - $30.75/hr

The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full-Time Clinical Research Coordinator 1 to work at the UHealth campus in Miami, Fl. CORE JOB SUMMARY The ...

University of Miami

Clinical Research Coordinator 1

Miami, FL · On-site

$23.25 - $30.75/hr

The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full-Time Clinical Research Coordinator 1to work at the UHealth campus in Miami, Fl. CORE JOB SUMMARY The Clinical ...

University of Miami

Clinical Research Coordinator 3

Miami, FL · On-site

$23.25 - $30.75/hr

Clinical Research Coordinator 3 The University of Miami/UHealth department of Neurology has an exciting opportunity for a Full Time Clinical Research Coordinator 3 to work at the UHealth Medical ...

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Full Time Clinical Research Informatics information

What is the difference between Full Time Clinical Research Informatics vs Clinical Data Analyst?

AspectFull Time Clinical Research InformaticsClinical Data Analyst
CredentialsTypically requires a degree in health informatics, computer science, or related field; certifications like CPHIMS are commonUsually holds a degree in health informatics, statistics, or related field; certifications are less common
Work EnvironmentWorks in clinical research settings, hospitals, or research organizations, focusing on data systems and EHR integrationWorks primarily with data analysis, reporting, and data management in healthcare or research settings
Employer & Industry UsageUsed by research institutions, pharmaceutical companies, and healthcare providers involved in clinical trialsEmployed across healthcare, research, and pharmaceutical industries for data management and analysis

Full Time Clinical Research Informatics focuses on managing and integrating clinical research data systems, requiring informatics expertise. Clinical Data Analysts primarily analyze and interpret data, often with less emphasis on informatics systems. Both roles overlap in data handling but differ in scope and technical focus.

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:
What cities in Florida are hiring for Full Time Clinical Research Informatics jobs? Cities in Florida with the most Full Time Clinical Research Informatics job openings:
Full Time Clinical Research Informatics jobs near you

CLINICAL RESEARCH COORDINATOR

Clinical Trials Investment Group

Miami, FL • On-site

$40K - $55K/yr

Full-time

Re-posted 8 days ago

Job description

Clinical Research Site seeking full time clinical research coordinator with experience. Must be Bilingual.

Responsibilities:

  • Must be able to manage an coordinate accordingly
  • Must provide clinical research support to investigators to prepare for and execute assigned research studies including, reviewing protocols, case report forms, study specific documents and electronic data capture systems use to record research data
  • Recruit and screen subjects for clinical trials and maintain all logs
  • Orient research subjects to the study
  • Design and maintain source documentation based on protocol requirements
  • Schedule and Execute study visits and perform all study procedures
  • Collect, Record and maintain research subject study data according to protocol and SOPS
  • Handle lab testing and analysis including preparation of specimen collection tubes and lab logistic
  • Monitor subject safety and report adverse reaction to appropriate medical personnel
  • Trouble shoot study related question and concerns and resolve all queries in a timely manner
  • Attend all IM, SIV and other training session required by the sponsor

Requirements:

  • Must be Bilingual ( English/Spanish)
  • 2+ years of Experience
  • Strong computer skills and knowledgable with medical terminology
  • Knowledge of Office 365
  • Excellent organization skills
  • Excellent written and oral communication skills
  • Excellent Time management
  • ICH and GCP certified

Company Description

WE ARE A GROWING COMPANY WITH VARIOUS DOCTORS SERVING AS PI IN DIFFERENT AREAS OF PRACTICE. WE SPECIALIZE IN CLINICAL TRIALS WE DO NOT OFFER REGULAR MEDICAL SERVICES.