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Research Assistant – On-site – Miami, Florida Clinical Research Organisation

Job in Miami, Miami-Dade County, Florida, 33222, USA
Listing for: Green Life Science
Full Time, Per diem position
Listed on 2026-10-17
Job specializations:
  • Healthcare
    Clinical Research
  • Research/Development
    Clinical Research, Research Assistant/Associate
Salary/Wage Range or Industry Benchmark: 18 - 22 USD Hourly USD 18.00 22.00 HOUR
Job Description & How to Apply Below
Research Assistant – On-site – Miami, Florida
Research Assistant (PRN)
Employment Type: PRN (As Needed)
Location: On-site – Miami, Florida
Compensation: $18.00-$22.00 per hour
About The Opportunity

Our client is a growing clinical research organisation that partners with pharmaceutical and biotechnology companies to conduct Phase I–IV clinical trials. With a strong focus on participant safety, quality, and regulatory compliance, the organisation offers healthcare professionals the opportunity to contribute to the development of innovative therapies in a collaborative clinical research environment.

Position Summary

The Research Assistant supports the successful execution of clinical research studies by assisting with participant visits, specimen handling, documentation, and study-related procedures. Working closely with the clinical research team, this individual helps ensure studies are conducted in accordance with study protocols, regulatory requirements, and internal quality standards.

Key Responsibilities
  • Prepare and maintain source documentation for participant study visits.
  • Perform protocol-required procedures including vital signs, ECGs, and phlebotomy.
  • Enter participant and study data accurately into research systems.
  • Manage laboratory kit inventory and maintain adequate study supplies.
  • Process, package, and ship laboratory specimens in accordance with protocol requirements.
  • Participate in study-specific and protocol training as assigned.
  • Assist with general administrative duties, including filing, scanning, copying, and maintaining study documentation.
  • Support the research team with additional study-related activities as required.
Qualifications

Education

  • High school diploma or equivalent required.
  • Associate’s or Bachelor’s degree in a healthcare or life sciences discipline is preferred.

Experience

  • Previous clinical, healthcare, or research experience is preferred.
  • Experience performing basic clinical procedures such as phlebotomy, ECGs, or vital signs is advantageous.
Required Skills
  • Understanding of Good Clinical Practice (GCP), ICH guidelines, and applicable regulatory requirements is preferred.
  • Familiarity with medical terminology.
  • Strong organisational and time-management skills.
  • High level of accuracy and attention to detail.
  • Excellent written and verbal communication skills.
  • Ability to work effectively both independently and within a multidisciplinary team.
  • Willingness to work overnight shifts as required by study schedules
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