I am pharmacology postgraduate with 6 years of exeperience in pharmaceutical data abstraction and mining.
To seek and maintain full-time position that offers professional challenges utilizing interpersonal skills, excellent time management and problem-solving skills. Ability to handle multiple projects simultaneously with a high degree of accuracy. Dedicated researcher familiar data (pharmacology) curation protocols. Well-coordinated in handling study documentation and records. Skilled in providing strategic solutions and assessing project performance. Hands-on experience completing development research and leading detailed competitive assessments. Detail-oriented Clinical Research Associate well-versed in coordinating operations, managing sites and drafting detailed clinical reports. Knowledgeable about action planning, database locking and standard operating procedures. Supports participant recruitment and management to meet research objectives.
Graduated with 60 percentage taking Pharmacology as a Major. published 2 research articles.
• Hands on experience on drawing chemical structures
• Extracting data from full text documents that include Scientific Patents, Medicinal chemistry Journals and other relevant literature
• Examination of curated/annotated data from multiple sources that cover maximum scope and provided quality outcome specifications in preset format.
• Acted as Subject Matter Expert in area of expertise and shared insights which provide competitive advantage.
• Contributed to process improvements, suggested opportunities wherever required.
• Hypothesized and contributed towards automation initiatives.
• Gained comprehensive knowledge of Preclinical medicinal chemistry research, clinical trials and therapeutic area.
• Became familiar with tools and techniques to enable and accelerate data curation and/or annotation is an advantage.
• Streamlined internal workflows by automating data collection, analysis, and reporting tasks.
• Boosted team efficiency with rigorous attention to detail and adherence to deadlines when completing projects.
• Prepared detailed reports summarizing research findings and recommendations for further action.
• Collaborated with cross-functional teams to generate relevant insights from diverse datasets.
• Increased client satisfaction by providing customized research solutions tailored to their unique business needs.
• Mentored new hires during their onboarding period leading them towards successful integration into team.
• Stayed up-to-date with industry developments through regular participation in conferences and workshops, ensuring relevance of research outputs.
• Implemented quality control protocols to enhance accuracy of data and research results.
• Used varied statistical and data analysis techniques to draw conclusions from research.
• Participated in data mining activities to uncover insights from various sources.
• Conducted primary and secondary research to better understand customer needs and behaviors.
• Excerption of clinical research data from various pharmacology journals and patents according to protocol (SOPs).
• Assessed business requirements and recommended technical products and solutions to meet needs.
• Evaluated the quality, critical analysis of curated clinical research data from various Research and Review journals as well as patents.
• Documentation of compliance for the quality feedback. Worked on Markush enumeration with Marvin sketch in patents.
