Technical writing of clinical report forms which are required by clinical trial drug protocols; technical writing of clinical trial reports; drug research and development (for others)

Management assistance and consultation for clinical trials of investigational drugs, namely, arranging for sites to perform clinical trials, arranging for the import, packaging, shipping, labeling, and distribution of drugs and other investigational supplies to and from the clinical trial sites, arranging for the central collection of laboratory specimens from clinical trial sites, making any and all filings required by the food and drug administration for investigational new drugs and new drug applications, preparing statistical reports resulting from clinical trials; marketing of new drugs

Building inspection, namely, inspecting potential sites for hosting clinical trials