Clinical Research Monitoring (CRA)

Medix™

Orlando, FLFull-timePosted Apr 10, 2026

20–26 an hour

Behavioral Health Market Context

Apply Nowvia Jooble

Job Description

ce with study protocols.
Key Responsibilities:
Prepare visit-specific documentation and charts for the Clinical Research Coordinator
Assist in monitoring subject flow and subject care
Observe, assist, collect, and record data for follow-up visits
Administer required questionnaires to study participants
Request and manage medical records for Serious Adverse Event reporting
Process and ship laboratory biological samples
Obtain written re-consents from study participants when necessary
Complete sponsor-required training and certifications
Perform other duties as assigned
Minimum Qualifications:
Education:
High School diploma or equivalent with relevant experience (Required)
Ophthalmic experience (Preferred)
Experience/Skills:
Previous human subjects research (Required)
Experience with specimen collection/injections
Strong oral and written communication skills
Ability to deliver safe and appropriate patient care in accordance with study protocols
Detail-oriented with excellent organizational skills
Details:
Pay Rate: $20-$26/hr (Dependent on experience)
Hours: Monday - Friday; Normal Business Hours; Onsite 5 Days a Week
Duration: Direct Hire
Seniority level Associate
Employment type Full-time
Job function Research
Industries Research Services

#J-18808-Ljbffr Medix™

Qualifications

  • High School diploma or equivalent with relevant experience (Required)
  • Previous human subjects research (Required)
  • Experience with specimen collection/injections
  • Strong oral and written communication skills
  • Ability to deliver safe and appropriate patient care in accordance with study protocols
  • Detail-oriented with excellent organizational skills

Benefits

  • Your actual pay will be based on your skills and experience — talk with your recruiter to learn more
  • Base pay range $20.00/hr - $26.00/hr
  • Pay Rate: $20-$26/hr (Dependent on experience)
  • Hours: Monday - Friday; Normal Business Hours; Onsite 5 Days a Week

Responsibilities

  • We are seeking a Clinical Research Assistant to support our team in conducting high-quality research studies while ensuring patient safety and compliance with study protocols
  • Prepare visit-specific documentation and charts for the Clinical Research Coordinator
  • Assist in monitoring subject flow and subject care
  • Observe, assist, collect, and record data for follow-up visits
  • Administer required questionnaires to study participants
  • Request and manage medical records for Serious Adverse Event reporting
  • Process and ship laboratory biological samples
  • Obtain written re-consents from study participants when necessary
  • Complete sponsor-required training and certifications
  • Perform other duties as assigned


More Jobs