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

  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

 

^*We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO), and the California Fair Chance Act (CFCA).

^*As a job position within our Clinical Sciences division, a successful completion of a background check may be required as a condition of employment. This requirement is directly related to essential job functions including but not limited to: high-risk working environments (laboratories, clinical settings), handling hazards chemicals or lab specimens, conducting direct patient care, accessing medical and confidential records, access to prescription medication or other drugs, and job duties that can cause serious injury or death as a result of error. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.