Pratik Rele

Pratik Rele

Associate Director, Data Science And Operational Excellence @ BeiGene

About Pratik Rele

Pratik Rele is the Associate Director of Data Science and Operational Excellence at BeiGene, with extensive experience in clinical data management and statistical programming.

Company

Pratik Rele currently works at BeiGene, serving as the Associate Director of Data Science and Operational Excellence. He joined BeiGene in 2020 and worked as a Senior Manager in the same department for two years before being promoted to his current role.

Title

Pratik Rele holds the position of Associate Director, Data Science and Operational Excellence at BeiGene. His role involves leveraging data science methodologies and operational strategies to drive performance and efficiency within the organization.

Previous Roles at Amgen

Pratik Rele held multiple roles at Amgen from 2011 to 2020. He served as Sr. Manager Medical Operations, Clinical EDC Study Design Operations Lead, eCOA/ePRO Technical Specialist, Clinical Data Management Process Efficiency Lead, CDM Systems Manager (EDC Operations Mgr), Clinical Data Management Systems Manager and RAVE Technical Specialist/SME, Study Event Naming Standardization Specialist, SAS Programmer-II, and Project Lead. These roles were primarily based in Thousand Oaks, California.

Education and Expertise

Pratik Rele achieved a Master of Science degree in Biostatistics from San Diego State University, where he also worked as a SAS Programmer/Graduate Research Assistant. He holds a Master of Science degree in Statistics from the University of Mumbai. He is certified in Base SAS 9.1 and holds an RAVE SDBE Certification. His technical skills span statistical programs (SAS, R, SPSS, Minitab, Matlab), programming languages (C, C++, SQL), and clinical databases (RAVE Safety Gateway, eClinical, Argus).

Technical Skills and Tools

Pratik Rele is proficient in using various applications and tools for project management and data analysis, including Spotfire, JIRA, Microsoft Project, MS Office, MS Access, SharePoint, and LaTeX. His deep knowledge in clinical standards encompasses GCP, ICH, CFR, CDISC, SDTM, ADAM, MedDRA, and WHOdrug, which underscores his expertise in clinical research processes and standards.

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