Purvi Kalra (Csm®)
About Purvi Kalra (Csm®)
Purvi Kalra is a Manager of Biostatistics and Programming at Ephicacy in India, where she has worked since 2023. She has a strong background in biostatistics and programming, with experience in various roles across multiple organizations since 2005.
Work at Ephicacy
Purvi Kalra has been serving as the Manager of Biostatistics and Programming at Ephicacy since 2023. In this role, she oversees biostatistical analysis and programming efforts, contributing to the company's projects in the pharmaceutical sector. Her responsibilities include managing statistical data models and ensuring compliance with regulatory standards.
Previous Employment History
Prior to her current position, Purvi Kalra held various roles in the biostatistics field. She worked as a biostatistician at Manipal Acunova from 2007 to 2009. She also served as a Statistical Programmer 2 at IQVIA from 2019 to 2020 and as a Senior Statistical Programmer at the same company from 2020 to 2023. Additionally, she was employed at Veeda Clinical Research as a biostatistician from 2005 to 2006 and at PharmaNet/i3 as an Associate Statistical Programmer from 2010 to 2014. She also worked as a freelancer from 2014 to 2019.
Education and Expertise
Purvi Kalra earned her Master of Science in Statistics from Gujarat University, where she studied from 2004 to 2006. Her academic background provides a strong foundation for her extensive experience in SAS programming and the implementation of statistical data models in the pharmaceutical industry.
Freelance Work and Training
In addition to her roles in various organizations, Purvi Kalra works as a freelance clinical research trainer. She provides training in biostatistics and programming, sharing her knowledge and expertise with professionals in the field. Her freelance work complements her extensive experience in the pharmaceutical industry.
Skills and Specializations
Purvi Kalra possesses extensive skills in SAS programming, macro writing, and report generation. She is involved in validation and regulatory affairs, ensuring that statistical analyses meet industry standards. Her expertise is particularly valuable in the context of clinical research and biostatistics.