Clinical Research Coordinator

6 days ago


Houston, Texas, United States MD Anderson Center Full time
Clinical Studies Coordinator Job Description

The Clinical Studies Coordinator is a key member of the research team at MD Anderson Center, responsible for the effective operation of designated protocols. This role involves development, design, and resolution of operations and budget issues in collaboration with the principal investigator or study sponsor.

Key Responsibilities:
  • Train other support staff in study coordination, providing training and guidance on policies and procedures related to clinical trials.
  • Coordinate FDA submissions and supervise clinical trials audits.
  • Perform QA audits to monitor compliance and accuracy of data.
  • Compile protocol data for manuscript submission.
  • Assist with supervisory functions and participate in the evaluation process.
Requirements:
  • Bachelor's degree.
  • Five years of experience in research study or direct patient care, with a preferred Master's degree.
Preferred Qualifications:
  • Clinical research certification, such as SOCRA or CCRC.
Work Environment:

Onsite presence is required.



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