Harpreet Pruthi Email & Phone Number | - Over 12 years of experience in Pharmaceutical and Biotech industry which includes experience in SAS Programming, Clinical Trials and System Development. - Over 4 years of experience as a line manager for direct reports. - Experience managing contracts/projects outsourced to external partners and CROs. - Experience in managing teams of programmers working on multiple projects. - Experience in SAS/Base, SAS/Macros, SAS/Graph, SAS/Stat and ODS with proven skills in coding, testing, debugging, problem solving and generating reports. - Experience with FDA electronic regulatory submissions including study level, ISS and ISE analysis, based on CDISC (SDTM/ADaM) standards. - Experience working over a wide range of therapeutic areas Specialties: Statistical Programming Project Management Process Improvement Operations Software Development

Harpreet Pruthi

- Over 12 years of experience in Pharmaceutical and Biotech industry which includes experience in SA...
Greater Boston, Greater Boston, United States

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Harpreet Pruthi’s Location Greater Boston, Greater Boston, United States

Harpreet Pruthi’s Current Industry Sanofi

Harpreet Pruthi’s Prior Industry Alexion Pharmaceuticals | Synageva Biopharma | Parexel | Pfizer | Eliassen

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Associate Director, Statistical Programming

2017-01-01 00:00:00 - Present

Associate Director, Statistical Programming

2015-09-01 00:00:00 - 2016-12-01 00:00:00

Associate Director, Statistical Programming

2014-09-01 00:00:00 - 2015-09-01 00:00:00

Manager, Statistical Programming, Global Data Operations

2012-06-01 00:00:00 - 2014-08-01 00:00:00

Manager, Clinical Programming

2008-08-01 00:00:00 - 2012-06-01 00:00:00

Manager, SAS Programming

2006-04-01 00:00:00 - 2008-08-01 00:00:00

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Harpreet Pruthi is a - Over 12 years of experience in Pharmaceutical and Biotech industry which includes experience in SAS Programming, Clinical Trials and System Development. - Over 4 years of experience as a line manager for direct reports. - Experience managing contracts/projects outsourced to external partners and CROs. - Experience in managing teams of programmers working on multiple projects. - Experience in SAS/Base, SAS/Macros, SAS/Graph, SAS/Stat and ODS with proven skills in coding, testing, debugging, problem solving and generating reports. - Experience with FDA electronic regulatory submissions including study level, ISS and ISE analysis, based on CDISC (SDTM/ADaM) standards. - Experience working over a wide range of therapeutic areas Specialties: Statistical Programming Project Management Process Improvement Operations Software Development