Senior Clinical Trials Coordination Lead

Miami Neuroscience Institute Baptist Health South Florida

Miami (FL)

On-site

USD 70,000 - 90,000

Full time

3 days ago
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Job summary

Miami Neuroscience Institute at Baptist Health South Florida is seeking a Senior Clinical Research Coordinator to independently manage complex trials, ensure protocol adherence, and coordinate activities with investigators, sponsors, and IRBs.

The role involves patient recruitment, data management, regulatory compliance, and training junior staff in GCP and study procedures. Flexibility for adjusted hours and bilingual communication is valued.

Qualifications

  • Requires pediatric clinical research experience and strong communication.
  • Certification in clinical research (CCRC/CCRP/CRA) and IATA preferred.
  • Bilingual in English/Spanish with excellent interpersonal skills.
  • Experience with IRB submissions and regulatory document management.

Responsibilities

  • Assists management with business development efforts.
  • Attends investigator meetings, pre-study visits, and initiation meetings.
  • Collects and maintains accurate patient data for sponsor submissions.
  • Communicates study objectives to hospital units and PI, sponsors, and monitors.
  • Schedules and facilitates study monitor visits and PI-sponsor communications.
  • Ensures compliance with research finance policies and reporting.
  • Interacts with patients to recruit subjects and monitor enrollment.
  • Utilizes Good Clinical Practices and FDA guidelines in trial conduct.

Skills

Bilingual English/Spanish
Pediatric clinical research
Strong communication
Regulatory compliance

Education

Bachelor's degree
Associate's degree

Tools

CTMS familiarity

Job description

Miami Neuroscience Institute at Baptist Health South Florida is seeking a Senior Clinical Research Coordinator to independently manage complex trials, ensure protocol adherence, and coordinate activities with investigators, sponsors, and IRBs.

The role involves patient recruitment, data management, regulatory compliance, and training junior staff in GCP and study procedures. Flexibility for adjusted hours and bilingual communication is valued.

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