Deepa Ailavarapu

• Reviewed medical records for accuracy of source documentation prior to database lock.
• Assisted in preparing periodic reports summarizing progress of clinical studies.
• Reviewed CRFs for completeness and accuracy before database entry.
• Monitored patient safety during clinical trials according to established guidelines.
• Organized, analyzed and modeled study data.
• Adhered to standards in areas involving data collection, research protocols, and regulatory reporting.
• Took vital signs and collected medical histories as part of study protocols.
• EDS,OneNote

• Demonstrated ability to attain and maintain a working knowledge of Good Clinical Practices and applicable Standard Operating Procedures
• Project management experience including the ability to prioritize, plan & evaluate deliverables; is well organized and structured, strong attention to detail
• Good computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software
• Demonstrated ability to attain and maintain a working knowledge of GCPs ,FDA , ICH, AE, SAE reporting and applicable SOPs

• Evaluated existing processes and proposed improvements to increase efficiency.
• Participated in cross-functional teams to review product specifications or requirements for completion of projects.
• Prepared samples for analysis using various techniques such as chromatography and spectroscopy.
• Developed and optimized novel formulations of drugs for clinical trials.
• Teamwork

Chemistry and Molecular Biology Laboratory Research expertize.

Drug discovery Laboratory Techniques.Implementation of previous role as Research Scientist.