Medix™
Lead Clinical Research Coordinator - 248982
Medix™, San Diego, California, United States, 92189
Lead Clinical Research Coordinator - 248982
Job Title:
Lead Clinical Research Coordinator
Pay Range:
$37.00/hr - $45.00/hr
Schedule:
Monday-Friday, 8:00 AM-4:30 PM
Position Summary:
The Lead Clinical Research Coordinator (Lead CRC) is responsible for managing and executing industry-sponsored clinical trial protocols within a hospital setting. This role serves as a critical link between patient care and scientific data collection, ensuring all research activities are conducted in compliance with regulatory, safety, and ethical standards. The Lead CRC provides hands‑on coordination of studies while supporting high-quality patient care and data integrity.
Key Responsibilities:
Lead and coordinate industry-sponsored clinical trials, including patient screening, enrollment, informed consent, and follow-up visits
Ensure study activities are conducted in accordance with protocol requirements, timelines, and sponsor expectations
Serve as a primary point of contact for investigators, sponsors, CROs, and internal hospital teams
Utilize clinical nursing skills to monitor and support research participants, with an emphasis on cardiac research studies
Conduct patient assessments, monitor safety parameters, and promptly report adverse events per protocol and regulatory requirements
Ensure participant safety, comfort, and adherence to study procedures throughout trial participation
Maintain strict adherence to Good Clinical Practice (GCP), institutional policies, and regulatory requirements
Ensure accurate, complete, and timely documentation of study data and regulatory files
Support audits, monitoring visits, and inspections as needed
Collect, process, package, and ship biological specimens in compliance with IATA Dangerous Goods regulations
Coordinate laboratory testing, supplies, and study materials to support protocol execution
Required Qualifications:
Active State of California RN or LVN license
Associate or Bachelor’s degree
Minimum of 2 years of experience working as a Clinical Research Coordinator on industry-sponsored clinical trials
Preferred Qualifications:
Experience in cardiac research
GCP (Good Clinical Practice) certification within the last two years (if not current, certification testing will be required after hire prior to participating in study protocols)
IATA Dangerous Goods certification within the last two years (if not current, certification testing will be required after hire prior to participation in studies involving laboratory testing)
Hospital-based clinical research setting
Collaborative, patient-centered environment with close interaction across clinical, research, and regulatory teams
Seniority Level:
Mid-Senior level
Employment Type:
Full-time
Job Function:
Health Care Provider and Research
Industries:
Hospitals and Health Care, Research Services, and Biotechnology Research
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Lead Clinical Research Coordinator
Pay Range:
$37.00/hr - $45.00/hr
Schedule:
Monday-Friday, 8:00 AM-4:30 PM
Position Summary:
The Lead Clinical Research Coordinator (Lead CRC) is responsible for managing and executing industry-sponsored clinical trial protocols within a hospital setting. This role serves as a critical link between patient care and scientific data collection, ensuring all research activities are conducted in compliance with regulatory, safety, and ethical standards. The Lead CRC provides hands‑on coordination of studies while supporting high-quality patient care and data integrity.
Key Responsibilities:
Lead and coordinate industry-sponsored clinical trials, including patient screening, enrollment, informed consent, and follow-up visits
Ensure study activities are conducted in accordance with protocol requirements, timelines, and sponsor expectations
Serve as a primary point of contact for investigators, sponsors, CROs, and internal hospital teams
Utilize clinical nursing skills to monitor and support research participants, with an emphasis on cardiac research studies
Conduct patient assessments, monitor safety parameters, and promptly report adverse events per protocol and regulatory requirements
Ensure participant safety, comfort, and adherence to study procedures throughout trial participation
Maintain strict adherence to Good Clinical Practice (GCP), institutional policies, and regulatory requirements
Ensure accurate, complete, and timely documentation of study data and regulatory files
Support audits, monitoring visits, and inspections as needed
Collect, process, package, and ship biological specimens in compliance with IATA Dangerous Goods regulations
Coordinate laboratory testing, supplies, and study materials to support protocol execution
Required Qualifications:
Active State of California RN or LVN license
Associate or Bachelor’s degree
Minimum of 2 years of experience working as a Clinical Research Coordinator on industry-sponsored clinical trials
Preferred Qualifications:
Experience in cardiac research
GCP (Good Clinical Practice) certification within the last two years (if not current, certification testing will be required after hire prior to participating in study protocols)
IATA Dangerous Goods certification within the last two years (if not current, certification testing will be required after hire prior to participation in studies involving laboratory testing)
Hospital-based clinical research setting
Collaborative, patient-centered environment with close interaction across clinical, research, and regulatory teams
Seniority Level:
Mid-Senior level
Employment Type:
Full-time
Job Function:
Health Care Provider and Research
Industries:
Hospitals and Health Care, Research Services, and Biotechnology Research
#J-18808-Ljbffr