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ABOUT

We work with small and large pharmaceutical and biotechnology companies to provide statistical consulting and to summarize, analyse and report clinical trials.  Our top priority is the quality of our work, ensuring we give you the best statistical advice, and analyze your clinical data optimally, getting it right first time. There are lots of different ways to analyse a set of data. We can advise on how to get the most out of your data. Statistics is an art!

We can work with our own internal systems and processes or seamlessly incorporate with your teams. We can manage and deliver whole clinical trial programs, or give you advice on a trial you are planning.

Team
Our Core Team
Shekhar Alimineti, CEO

calimineti@deftconsultingcorp.com 

Shekhar has over 14 years of experience in clinical/statistical programming through positions in the bioscience industry (GlaxoSmithKline, Roche, Seattle Genetics) and at consulting and CRO firms (Clinforce, SmithHanely Consulting Group).  As a Deft Consultant he worked at various biotech companies such as Amgen, AstraZeneca and Biogen. He has experience managing and leading programming efforts on various Phase I through III studies and several NDAs and BLAs.  Shekhar's primary areas of expertise are in programming process development and standards and in CDISC data standards implementation.

Haritha Mogulla

Principal Programmer

Haritha is a statistical programming consultant with over 10 years of experience in clinical research settings (AstraZeneca, Pfizer, Roche). Through working on phase I-IV clinical studies in various therapeutic areas, she has developed strong SAS programming skills and knowledge on statistical programming process, CDISC standards, and electronic submissions. Projects have included analysis files/tables/listings/graphs creation, system validation, utility macro development, and integrated safety database creation for BLA/NDA.

Pavan Kumar

Sr. Programmer/Analyst

Pavan has just over 12 years of experience in both pharmaceutical and biotech setting. He has excellent experience in leading Clinical Studies in Phases I through III. He has excellent understanding of CDISC submission standards including but not limited to SDMT, ADaM datasets generation, CDASH standards and define.xml

Need more details? Contact us

We are here to assist. Contact us by phone, email or via our Social Media channels.

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