Asma Khan Email & Phone Number

United States

United States

• Conducted advanced data analysis using SQL, improving research project outcomes.
• Optimized database performance through strategic indexing and query tuning.
• Designed robust database structures, enhancing scalability and data integrity.
• Automated data processes with SQL stored procedures and triggers.
• Presented complex research findings using Tableau to academic and professional stakeholders.

United States

Cambridge, Massachusetts, United States

• Assist in collecting, organizing, and maintaining clinical trial data.
• Input and manage data in electronic databases.
• Assist in preparing and organizing essential study documents, including consent forms, regulatory binders, and patient records.
• Help schedule patient visits and follow-ups as required by the study protocol.
• Support patient enrollment by explaining the study to potential participants under supervision.
• Assist in analyzing data under the guidance of senior researchers or data analysts.

• Managed clinical data collection and organization from EHRs and patient charts.
• Ensured data management practices adhered to regulatory standards.
• Developed reports for senior faculty and administrators to inform decision-making.

- Conducted daily concurrent reviews of inpatient records on assigned units to ensure complete and accurate physician documentation for compliant coding at discharge.- Performed initial code assignment for working DRGs, updated as necessary based on documentation and physician query responses. - Collaborated closely with coders, case managers, quality.

Karnataka, India

-As an Assistant Professor worked in conducting lectures, seminars, and workshops for undergraduate students.- Participated in departmental and university committees, as well as engaging in community service and outreach activities.- Performing administrative tasks related to teaching, research, and service, such as grading, course coordination.

- Design and develop Case Report Forms (CRFs) for clinical trials- Ensure accurate and efficient data collection processes- Manage electronic data capture (EDC) systems and databases- Perform data cleaning activities to identify and rectify data discrepancies- Conduct data validation checks to ensure data consistency and accuracy- Develop and implement.

- Monitor clinical trials to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.- Conduct site visits to assess protocol and regulatory compliance, data integrity, and patient safety.- Verify the accuracy and completeness of case report forms (CRFs) against source documents.- Ensure proper.