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How bacteria in tumors drive treatment resistance in cancer

Clinical Research Consent Writer - Clinical Trials Start-Up

MD Anderson Cancer Center is one of the world's most respected centers devoted exclusively to cancer patient care, research, education, and prevention. The Clinical Research Consent Writer is responsible for editing informed consent documents for clinical protocols to ensure compliance with federal regulations while making them comprehensible at a sixth- to eighth-grade reading level. This role involves collaboration with various departments to support study submissions and improve activation timelines.

Health Education Specialist

Education Specialist

Clinical Studies Coordinator - Pediatrics Patient Care

Technical Writing and Publications Manager for the Center for Goal Concordant Care Research

Research Care Coordinator/ Research Navigator

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