Clinical Research Coordinator — One Site, Impactful Trials

Trusted Medical PLLC; Florida; Hybrid; USD 70,000 - 100,000; Full time

Benefits offered by this job

Competitive compensation

Collaborative research team

Job summary

Trusted Medical PLLC seeks a seasoned Clinical Research Coordinator to manage studies from initiation to closeout at our Hialeah, FL site, with occasional hybrid scheduling. The role emphasizes recruitment, regulatory compliance, data integrity, and cross‑functional collaboration with investigators, sponsors, and national teams.

The ideal candidate has 5+ years of clinical research experience, strong knowledge of FDA regulations and GCP, and a DEA-friendly, patient-centered approach to trials

Qualifications

• Bachelor’s degree in a healthcare field is required.
• Minimum 5 years of clinical research experience.
• Experience supporting multiple clinical trials and regulatory documentation.
• Strong knowledge of FDA regulations, GCP, IRB requirements, and study protocols.

Responsibilities

• Coordinate studies from start-up through closeout.
• Support participant recruitment, enrollment, retention, and visits.
• Maintain accurate regulatory files, study records, and data.
• Monitor timelines, milestones, and protocol compliance.
• Ensure compliance with FDA regulations, GCP, IRB, and sponsor guidelines.
• Collaborate with investigators, sponsors, CROs, and leadership.
• Support monitoring visits, audits, and regulatory activities.
• Assist with data collection, review, and discrepancy resolution.
• Support study budgets, site operations, and trial activities.

Skills

Regulatory compliance

Clinical communication

Study coordination

Team collaboration

Education

Bachelor’s degree in Nursing, Life Sciences, Public Health, Healthcare Administration, or related field

CCRP/CCRC or equivalent certification

Tools

EDC platforms

Clinical research systems

Job description

Trusted Medical PLLC seeks a seasoned Clinical Research Coordinator to manage studies from initiation to closeout at our Hialeah, FL site, with occasional hybrid scheduling. The role emphasizes recruitment, regulatory compliance, data integrity, and cross‑functional collaboration with investigators, sponsors, and national teams.

The ideal candidate has 5+ years of clinical research experience, strong knowledge of FDA regulations and GCP, and a DEA-friendly, patient-centered approach to trials