Research Assistant – On-site – Miami, Florida Clinical Research Organisation
Listed on 2026-10-17
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Healthcare
Clinical Research -
Research/Development
Clinical Research, Research Assistant/Associate
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 SummaryThe 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.
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.
- 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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