HARSHAVARDHAN PRATHIPATI

REPORTS:

• Performed system analysis, documentation, testing, implementation, and client support for multiple projects.
• Medical patient profile report
• Metadata Report
• Coding Medical Report
• TPV Data Processing Report
• Adjudication Report
• Scan Tool Report
• SAE Merge report
• Vendor Reconciliation Report
• Dataset Count Report
• Other Ad‑hoc Report
• Merge issue Report

EDIT CHECKS:

• E-crf checks.
• TPV reconciliation checks.
• IPD Listings.
• TPV Structural checks, Import setup, Processing
  MSS (LB listings)Identified and resolved problems through root cause analysis and research.
• Performed system analysis, documentation, testing, implementation, and user support for multiple projects.
• Recommended process improvements to continually identify, analyze and fix constraints and challenges.
• Apart from regular responsibilities been a active member of the Global Initiative team and contributed the team with multiple initiative works (Merged reports, Custom reports, patient profile report).

Other skills:

• Good Knowledge of Clinical Trial Domain regarding Drug, Design, Dosage & Development, Trial‑Phases, Designs, Protocol, ICH‑GCP, 21 CFR Part 11, ICF,
  CRF, aCRF , SAP
• Good knowledge of clinical data management
  Experience in producing HTML, RTF, PDF formatted reports using SAS/ODS.
• Good knowledge in importing multiple formatted files by using SAS import methods like PROC IMPORT, INFILE Statements.
• Experience of using SAS functions and key options.
  Experience generating reports using SAS procedures PROC REPORTS.
• Good knowledge of statistical procedures like PROC MEANS, PROC TRANSPOSE, PROC FREQ, PROC SUMMARY, PROC COMPARE.
• Good knowledge of implementing Macros and PROC SQL techniques.
• Completed all my studies within the projected timelines and budget with high quality.
• As a study lead programmer performed all the activities and completed the study without any standard deviations.