Provides support to the cancer center academic and research mission as a scientific writer and editor for grant proposals and projects, articles for publication including white papers, and lectures and presentations. May provide support to the cancer center interdisciplinary clinical trials teams by collaborating with individual investigators to produce high quality clinical trials including case reports forms and informed consent forms, assuring compliance with federal regulations, i.e., develop protocol templates that meet required elements of the FDA, NIH, University review committees and other regulatory agencies. Works with the department's research administration team regarding research grant projects. Reviews and analyzes federal regulations regulating the conduct of research. Performs related responsibilities as required.
MINIMUM QUALIFICATIONS: Master's Degree and three years of scientific writing experience including contributions to articles published in scientific journals and formal papers, or an equivalent combination of experience, education and training.