Clinical Protocol Writer I - Research & Trials

A leading cancer research institution in Tampa, Florida, is looking for a Protocol Writer to contribute to early phase clinical trials. You will collaborate with investigators to prepare clinical trial protocols that adhere to regulatory standards. The ideal candidate should have a strong scientific background, at least two years of medical writing experience, and the ability to manage multiple projects effectively. This role offers a full-time schedule and the opportunity to contribute to cancer research efforts.
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