Clinical Protocol Writer I – Early-Phase Trials

A leading cancer research institution in Florida is seeking a Clinical Research Protocol Writer. The role involves writing, editing, and completing clinical trial protocols, working with clinical investigators to ensure submission to the Scientific Review Committee. Candidates should have at least 2 years of medical writing experience and a strong background in clinical research. This position offers the opportunity to contribute to groundbreaking trials and work within a recognized institution committed to cancer prevention and cure.
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