Clinical Research Coordinator II Pulmonology

Lumiresearch; Dallas, Northern (TX, KY); Hybrid; USD 60,000 - 75,000; Full time

Job summary

Lumiresearch is seeking a Clinical Research Coordinator II for pulmonology in the Greater Dallas–Fort Worth area. The role emphasizes patient coordination, regulatory and administrative compliance, study initiation, and accurate adverse event reporting.

The ideal candidate has a Bachelor’s degree and 3+ years of clinical trial or related clinical experience, with pulmonology exposure and phlebotomy skills considered a plus. Strong MS Office proficiency is required.

Qualifications

• Bachelor’s degree and at least three years of clinical trial or related clinical experience.
• Pulmonology clinical research experience required.
• Phlebotomy skills are a plus.

Responsibilities

• Coordinate and attend study initiation visits and manage patient activities throughout enrollment.
• Maintain regulatory files, source documentation, and manage adverse events reporting.
• Educate patients on trial requirements and assist with informed consent processes.
• Collaborate with investigators, clinic staff, and external partners to ensure smooth trial operations.

Skills

Clinical trial management

Regulatory compliance

Patient coordination

Operational problem-solving

Team collaboration

Education

Bachelor's degree

Tools

MS Office

Job description

Clinical Research Coordinator II Pulmonology

This Clinical Research Coordinator II role seeks a highly organized, detail-oriented professional to manage essential aspects of clinical trials. You’ll play a crucial role in patient coordination while assisting in regulatory and administrative compliance, study initiation, maintaining documentation, and accurately reporting adverse events.

The ideal candidate possesses strong communication, critical thinking, and problem-solving skills, with proficiency in MS Office. A Bachelor’s degree and at least three years of combined clinical trial or relevant clinical work experience are required. Pulmonology experience required and phlebotomy skills are a plus.

Qualifications:

• Comprehensive Clinical Trial Management:Proven ability to coordinate and attend study initiation visits, manage all patient activities throughout trial enrollment, and ensure meticulous collection and documentation of source data, including adverse events.
• Expert Regulatory Compliance & Data Integrity:Skilled in maintaining current protocol documentation, managing regulatory files in SharePoint, utilizing Electronic Data Capture (EDC) systems, and addressing monitor queries to ensure data quality and compliance.
• Patient-Centric Coordination & Communication:Proficient in performing informed consent for diverse populations, educating patients on trial requirements, coordinating complex research visits (screening, treatment, tissue collection), and maintaining optimal patient tracking.
• Operational Acumen & Problem-Solving:Adept at creating and following logistical processes for patient onboarding, developing organized source documentation, and applying critical thinking to resolve logistical challenges efficiently.
• Team Collaboration & Technical Proficiency:Effectively collaborates with senior CRCs, investigators, clinic staff, and external partners. Proficient in MS Office tools for communication and organization, with the ability to learn new patient registering systems quickly.

Education: Bachelor’s degree
Location: Greater Dallas-Fort Worth area
Experience: 2-3 years of pulmonology clinical research experience required.