Medix™
This range is provided by Medix™. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $65,000.00/yr - $75,000.00/yr
Recruitment Advisor II - National Clinical Research/National Life Sciences at Medix™ | I hire Clinical Research professionals across the U.S., Puerto… 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
Seniority level Not Applicable
Employment type Full-time
Job function Research
Industries Research Services
Medical insurance Vision insurance
401(k)
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Base pay range $65,000.00/yr - $75,000.00/yr
Recruitment Advisor II - National Clinical Research/National Life Sciences at Medix™ | I hire Clinical Research professionals across the U.S., Puerto… 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
Seniority level Not Applicable
Employment type Full-time
Job function Research
Industries Research Services
Medical insurance Vision insurance
401(k)
#J-18808-Ljbffr