• Review source materials such as Clinical trial registry updates, Pharma / biotech press releases, Medical or scientific publications, Conference abstracts, Regulatory updates, Patent updates, Company pipeline or asset updates, Medical affairs or drug safety updates, Product, indication, or development milestone announcements. • Determine whether the item should be included in a weekly monitoring report. • Apply clear inclusion / exclusion criteria. • Identify the relevant company, product, asset, indication, mechanism of action, study, or update. • Summarize the key information in concise, source-grounded language. • Verify claims against the original source. • Flag ambiguity, missing information, or uncertain relevance. • Maintain structured data in a consistent format. • Perform quality checks for accuracy, completeness, and clarity.