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Clinical Research Coordinator - 245198

Clinical Research Coordinator - 245198

MedixOcala, FL, United States
3 hours ago
Job type
  • Full-time
Job description

Position Overview

As a Respiratory / Pulmonary Clinical Research Coordinator, you will be responsible for coordinating and executing respiratory-focused clinical trial activities. You will not have any leadership or supervisory duties—this role emphasizes hands-on support, participant care, data collection, and maintaining protocol fidelity.

Key Responsibilities

Clinical Duties (Respiratory / Pulmonary Focus)

  • Perform respiratory-specific assessments—pulmonary function testing (PFTs), DLCO, cardiopulmonary exercise testing, etc.—as required by protocols.
  • Conduct essential clinical procedures : obtaining vital signs, 12-lead ECGs, phlebotomy, and other protocol-specific tasks.
  • Prepare and manage study-related materials, including lab kits, research supplies, and required documentation for visits.

Study Coordination & Data Management

  • Schedule, confirm, and coordinate participant visits in alignment with protocol timelines and team availability.
  • Record and maintain high-quality data in source documents and CRFs; process data entry promptly and accurately.
  • Assist in QC / QA processes : review and correct documentation in line with ALCOA-C principles or site SOPs.

    • Participant Coordination

  • Serve as a friendly point of contact for research participants, ensuring positive, efficient, and respectful patient experiences.
  • Support in obtaining informed consent and managing participant eligibility screening (as applicable, depending on site protocol).
  • Maintain inventory and manage research supply needs in coordination with site SOPs .

    • Compliance & Monitoring Support

  • Ensure adherence to site SOPs, GCP, ICH, and FDA regulations throughout all trial-related activities.
  • Support for monitoring visits, audits, or regulatory inspections by preparing required documentation and responding to sponsor / CRO inquiries as needed.

    • Qualifications Required

  • Strong organizational skills and meticulous attention to detail.
  • Excellent interpersonal, verbal, and written communication abilities.

    • Preferred

  • Certification as a Clinical Research Coordinator (CCRC) or CCRP
  • At least 2 years of clinical research experience
  • Experience with medical terminology and knowledge of pulmonary clinical trial protocols and regulatory processes
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    Clinical Research Coordinator • Ocala, FL, United States