Cedars-Sinai - Montebello, CA

posted 7 days ago

Full-time - Mid Level
Montebello, CA
1,001-5,000 employees
Hospitals

About the position

As a Clinical Research Coordinator II at Cedars-Sinai, you will play a crucial role in coordinating clinical trials and research studies. This position involves working independently to screen potential patients, manage study documentation, and ensure compliance with regulatory standards. You will collaborate with physician-scientists and researchers to facilitate groundbreaking medical advancements and contribute to the overall success of clinical research initiatives.

Responsibilities

  • Schedule patients for research visits and procedures.
  • Document changes in patient condition, adverse events, and protocol compliance on Case Report Forms (CRFs).
  • Maintain accurate source documents related to all research procedures.
  • Participate in monitoring and auditing activities.
  • Notify direct supervisor about concerns regarding data quality and study conduct.
  • Work closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit necessary reports.
  • Assist with patient research billing and reconciliation.
  • Maintain research practices using Good Clinical Practice (GCP) guidelines.
  • Ensure strict patient confidentiality according to HIPAA regulations.
  • Coordinate training and education of other personnel.
  • Identify quality and performance improvement opportunities.

Requirements

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

Benefits

  • Competitive salary ranging from $71,760.00 to $100,000.00.
  • Opportunities for professional development and training.
  • Access to cutting-edge research and clinical trials.
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