- Preparation of reports in English language using Microsoft Office.-Conduction of extensive analysis using official and unofficial sources of information, such as regulatory information provided by local Ministries of Health, including approvals, submissions and rejections, clinical trials, public tenders, patents, DMFs, GMP certificates and international trade operations.-Development of forecast & approval timelines for pharmaceutical products in the global market.-Market research and competitive intelligence of the pharmaceutical industry, focusing on customer requirements. -Monitoring of global development activities of pharmaceutical active ingredients and finished formulations.