Clinical Research Associate

7 days ago


Glendale, California, United States Medix™ Full time
Clinical Research Coordinator

Medix™ is seeking a highly skilled Clinical Research Coordinator to join our team. As a Clinical Research Coordinator, you will play a critical role in the success of our clinical trials.

Key Responsibilities:
  • Screen potential patients for protocol eligibility and present non-medical trial concepts and details.
  • Participate in the informed consent process and ensure accurate and timely source documents, data collection, documentation, entry, and reporting.
  • Compile and report on each study, including information related to protocol activity, accrual data, workload, and other research information.
  • Ensure compliance with all federal and local agencies, including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).
Requirements:
  • 2+ years of experience working as a Clinical Research Coordinator.
  • Bachelor's degree in a related discipline.
  • Oncology trial experience is a plus.

As a Clinical Research Coordinator at Medix™, you will have the opportunity to work on a variety of clinical trials and contribute to the development of new treatments and therapies. If you are a detail-oriented and organized individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.



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