With a strong research background, I’ve screened over 2,500 research papers and extracted data from more than 800 studies. I’m skilled in using databases such as PubMed, Cochrane Library, Scopus, ClinicalTrials.gov, the WHO ICTRP, and disease burden databases to source high-quality literature and evidence. My hands-on experience includes working on two live industrial projects and one freelance assignment, covering a wide spectrum of topics such as: • Blog Writing, Presentations, Content Strategy • Evidence Synthesis and Evidence-based decision-making • Health technology assessments (HTA) • Competitive intelligence and pipeline analysis • Epidemiology studies and market research • Indexed and summarized scientific data from research journals, patents, and articles. • Organized information for easy retrieval and analysis. • Analysed data related to drugs, drug targets, and regulatory information. • Collected clinical and pre-clinical data from multiple scientific sources. • Entered and structured this data into relevant databases. • Reviewed data for accuracy and completeness. • Screened scientific journals to identify biomarkers. This multidisciplinary exposure allows me to deliver writing that is not only technically sound but also aligned with strategic goals and industry standards. Whether it's regulatory writing, medical communications, or scientific content development, I bring clarity, precision, and depth to every project.