Experience must include a minimum of 12 months postmarketing epidemiology studies, surveillance, andor trials in the pharmaceutical industry, biotechnology industry, or academic research setting; integration of concepts and guidelines such as those from FDA, EMA, public health agencies, nongovernmental organizations, and clinical practice groups for generation of realworld evidence in pharmacoepidemiology; databases commonly used in epidemiological research e.g., Clinical Practice Research Datalink, Marketscan, Optum; standard and advanced statistical analysis methods; and analyses using software packages such as R, SQL, and relevant platforms. Experience may be gained concurrently.
Categories: eb3
0 Comments