Pulmonology Clinical Research Coordinator II

Lumi Research; United States; On-site; USD 55,000 - 85,000; Full time

Benefits offered by this job

Two weeks (80 hours) PTO annually

Monthly medical benefits stipend

Clinical research certification"

Job summary

Lumi Research in the United States is seeking a Clinical Research Coordinator II (CRC II) in Pulmonology to support patient enrollment and trial execution.

You will handle regulatory documentation, patient consent, data collection, and monitoring visits, collaborating with clinicians and sponsors. This full-time role requires a Bachelor’s degree and at least two years of pulmonology or clinical trial experience.

Qualifications

• Bachelor’s degree (degree verification required).
• Minimum two years in pulmonology clinical settings or clinical trial research.
• Experience with regulatory coordination and patient consent.
• Eligible to work in the United States.

Responsibilities

• Coordinate study initiation visits and planning meetings.
• Maintain study protocols and regulatory documentation.
• Collect source data and enter data into EDC systems.
• Conduct informed consent under supervision and educate patients on trial requirements.
• Monitor patient activities and manage adverse events reporting.
• Support PI oversight with patient tracking and sponsor updates.

Skills

Critical thinking

Problem-solving

Professional communication

Organizational skills

Multitasking

Microsoft Office

Microsoft Teams

Education

Bachelor's degree

Tools

EDC systems

Regulatory databases

Job description

Lumi Research in the United States is seeking a Clinical Research Coordinator II (CRC II) in Pulmonology to support patient enrollment and trial execution.

You will handle regulatory documentation, patient consent, data collection, and monitoring visits, collaborating with clinicians and sponsors. This full-time role requires a Bachelor’s degree and at least two years of pulmonology or clinical trial experience.