Shiva Kumar
Experience: 18 years Statistical Programming Experience; Deep understanding and implementation of advanced SAS, R and python on clinical trial data (P1-P3); Experience with several other tools used in the industry; Regulatory submission experience (FDA, PMDA, EMA); Strong understand of the drug development process; tools design; Data management proficiency including cleaning, transformation and integration from multiple sources. Also one of the founders of FUSIONDATAPRO, a consulting firm in the US catered for clinical trial delivery, and also the founding member of PACEDO technologies
Praveen Kumar (PG)
Experience: 14 years of experience in the US Pharma/Biotech/CRO industry; Experience in leading programming teams, mentoring staff and providing technical expertise and guidance; through with the latest industry trends, technologies, best practices in clinical data analysis; innovative solutions to improve process and workflows; Strong track record of successful project delivery, a deep understanding of the drug development process and the ability to provide mentorship and leadership within the teams.
Santosh Kumar
Experience: 13 years’ experience in the in the US Pharma/Biotech/CRO industry; SME in the clinical data standards space from clinical data design to standardization and transformation of data; Extensive experience in analysis, design, and development of applications, reporting and modeling in SAS and R programming in all phases of clinical trials.
Vijaya P
With more than 10 years of experience in the US as a statistical programmer, Vijaya has excelled in the space of using SAS tool both base and advanced. Currently she as an SME works as a SAS consultant. She also has a PhD from Indian Council of medical research.
Deepika K
An R expert who is currently designing and validating tools/packages based on R within the firm she is working for.
Kaylan B
A clinical trials programming professional working for an reputed Pharma company, with 11 + years of end-to-end Study lead experience in leading programming activities for regular and complex Clinical Trials (RWE, DTH, Registry). An SME for CDASH, CDISC, implementation from raw database design to SDTM, ADAM, Analysis and Reporting in clinical trials for successful regulatory agencies submissions.
