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

Job Tags

Similar Jobs