Nikhil Wagh

About Nikhil Wagh

I am a highly skilled and goal-oriented professional with a diverse background in the pharmaceutical and clinical research organization sectors. With over 12 years of experience, I specialize in utilizing SAS (9+) and BI tools to drive efficient data analysis, management, and reporting in the Clinical Trial Industry.My expertise lies in Clinical Data Analysis, where I excel in creating comprehensive summaries, listings, and graphs (TLFs) from clinical trial data. Leveraging my proficiency in Base SAS, SAS/SQL, SAS/Macro, SAS/ODS, SAS/Graphs, and SAS/Stat, I have consistently delivered accurate and insightful analyses that contribute to informed decision-making in clinical research.Throughout my career, I have honed my communication skills, enabling me to effectively collaborate and build strong working relationships with cross-functional teams. I am equally comfortable working independently, taking ownership of projects, and driving them to successful completion.In addition to my extensive experience in data analysis and reporting, I possess exceptional process automation abilities that have consistently enhanced efficiency and productivity in my work. I have a proven track record of streamlining workflows and setting up new, efficient processes using verious SAS programming techniques.By leveraging my in-depth knowledge of SAS/MACROS, I have successfully automated repetitive and time-consuming tasks, allowing for faster turnaround times and improved accuracy. Whether it is data cleaning, transformation, or generating complex reports, my ability to create efficient SAS macros has significantly reduced manual effort and minimized the risk of errors.I take a meticulous approach to process improvement, carefully analyzing existing workflows to identify areas for automation and optimization. Through my expertise in SAS programming, I have successfully designed and implemented streamlined processes that have resulted in substantial time and cost savings for my organizations.As a process-oriented professional, I am always eager to explore new opportunities to optimize workflows and improve efficiency. If you are seeking a driven individual who can bring innovative ideas and automate processes, I would be delighted to connect with you.Let\'s collaborate to enhance productivity, drive efficiency, and achieve exceptional results through process automation in the Clinical Trial Industry and beyond!

Experience

1. Principal Clinical Programmer

   诺华

   Sep 2022 — Present

   Reporting & Analysis · R Shiny · Databases · Relational Databases · Data Reporting · SAS · R (Programming Language) · Qlik Sense · JReview · SQL · Spotfire · Python

Education

• North Maharashtra University

  Bachelor of Pharmacy - BPharm, Pharmaceutical Sciences

  2009

Skills

• Electronic Data Capture (Edc)
• Edc
• Ctms
• Lifesciences
• Cdisc
• Biostatistics
• Microsoft Office
• Clinical Trials
• Statistical Programming
• Good Clinical Practice (Gcp)
• U.s. Title 21 Cfr Part 11 Regulation
• Gcp
• 21 Cfr Part 11
• Clinical Data Management
• Oracle Clinical
• Data Analysis
• Sas
• Sas Base
• Protocol
• Spotfire
• Ich-Gcp
• Sas Programming
• Data Management
• Validation
• Clinical Research
• Pharmaceutical Industry
• Fda
• Life Sciences
• Macro
• Sql
• Sdtm
• U.s. Food and Drug Administration (Fda)