A Statistical Programmer in the pharma domain, with background in Biotechnology & Bioinformatics.
After gathering 4 years of experience in handling reporting activities on pharmacokinetic studies in the general medicines area, I moved to Oncology Full development in 2013 to check out the other end of the spectrum.
Over my years of working in this industry, along with increasing my skills as a SAS programmer, I have picked up knowledge and expertise in the area of PK studies, CDISC standardization, Biostatistics and the general conduct of clinical trials. Along with this, I have also dabbled in Trainings, and I have been part of teams developing & testing new tools for the Statistical Pr...
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