Sirimalla Jyothi

• Examined scientific research articles and patents, carefully searching for relevant data that is essential for gaining deeper understanding and exploring potential practical uses
• Analyzed both qualitative and quantitative data, resulting in detailed reports that present comprehensive findings to enhance understanding and inform decision-making
• Collected pertinent information from a diverse range of complete textual documents, including scientific journals, patents, and other relevant literature, with the goal of creating a comprehensive dataset for research and analysis
• Analyzed large volume of data to identify patterns, trends and correlations.
• Supported senior management in making informed decisions by delivering timely and accurate research findings.
• Created and maintained database to store research data.

• Conducted thorough secondary research on drug profiling, analyzing approval timelines, market launch strategies, sales performance, and patent expiry dates to gather crucial insights for informed decision-making and strategic-planning in the pharmaceutical industry
• Utilized patent databases (USPTO, EPO, and WIPO) to retrieve patent filings and expiration timelines, aiding strategic planning
• Assessed supplementary protection certificates (SPCs) and market exclusivity to predict potential generic market entry, supporting proactive business strategies
• Validated forecast models through stringent quality control methods to ensure accuracy and reliability, resulting in improved prediction dependability and informed decision-making based on verified estimations
• Participated in regular training sessions to stay current on industry trends, improving personal expertise and job performance.
• Developed a keen understanding of company KPIs, using this knowledge to guide accurate data interpretation and insightful analysis.

Performed thorough analysis of pharmaceutical data to update drug profiles within company databases (Cortellis, Recap IQ), ensuring accuracy and currency of information for informed decision-making and facilitating access to essential data for research, development, and operational activities

• Oversaw and updated company records, including pre-clinical, clinical, regulatory, financial, and deal-related changes ensuring accuracy and completeness through real-time quality checks
• Performed extensive research on FDA, EMA, Japan, and China regulatory websites to gather data on regulatory applications and updates for comprehensive regulatory analysis
• Reviewed various clinical trial databases regularly for new or missing information on current clinical studies and their results to ensure complete and up-to-date entries in the drug profile database
• Spearheaded initiatives aimed at improving overall team performance through continuous learning opportunities.
• Enhanced research quality by implementing rigorous data collection and analysis methodologies.