Pulmonary Research Program/Lung Institute Clinical Research Coordinator III

6 days ago

Los Angeles, California, United States CEDARS-SINAI Full time
About the Role

Cedars-Sinai is seeking a highly skilled Clinical Research Coordinator III to join our Pulmonary Research Program/Lung Institute team. As a key member of our research team, you will be responsible for providing study coordination, including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.

This position is responsible for the oversight of all studies with the group and the assignment of studies to clinical research personnel within the group, as well as supervision of research staff. The incumbent plans and coordinates strategies for growing research participant enrollment, improving efficiency, training of personnel, and identifying new research opportunities.

Key Responsibilities:

  • Scheduling of patients for research visits and procedures
  • Documentation of patient information, including changes in patient condition, adverse events, concomitant medication use, protocol compliance, and response to study drug
  • Maintenance of accurate source documents related to all research procedures
  • Accurate and timely data collection, documentation, entry, and reporting, including timely response to sponsor queries
  • Scheduling and participation in monitoring and auditing activities
  • Compilation and reporting of study information, including protocol activity, accrual data, workload, and other research information
  • Notification of supervisor regarding concerns regarding data quality and study conduct
  • Submission of Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines
  • Regulatory/Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation
  • Maintenance of research practices using Good Clinical Practice (GCP) guidelines
  • Maintenance of strict patient confidentiality according to HIPAA regulations and applicable law
  • Participation in required training and education programs
  • Supervision of other research staff

Requirements:

  • High School Diploma/GED, required
  • Bachelor's degree, preferred
  • 4 years of clinical research experience, required
  • ACRP/SOCRA (or equivalent) certification, preferred

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