Jeff Schumack has over 20 years of experience in the IT industry, mostly in the Biotechnology sector. His experience includes managing complex projects, leading multi-disciplinary teams, building validation programs in response to regulations including FDAs 21 CFR, Part 11, architecture and development of custom laboratory software, and a deep understanding of business processes used by Clinical Research & Development organizations.
Jeff was the Associate Director of Clinical & Regulatory Systems at Human Genome Sciences. In this role, Jeff directed the implementation of a Clinical and Regulatory informatics infrastructure to support HGS’ clinical trials. Jeff successfully implemented this program by working closely with all groups in the Research and Development Organization including; Clinical Data Management (Clintrial, Integic), Clinical Operations (CTMS), Clinical Immunology (CSTrack), Drug Safety (ARISg), Regulatory Affairs (Documentum and Insight Publisher) and Biostatistics (SCE). Jeff was instrumental in the creation of HGSs Computerized System Validation Program, serving as the lead IT interface for all validation activities. He authored several Policies and SOPs in support of this program. Jeff was also the lead IT contact on IT matters during FDA and partner audits.
While a majority partner at TSI Consulting, Inc., Jeff managed several client accounts providing IT services to Biotechnology companies. He and his team developed custom applications for various clients including companies performing Biologic testing and Genomic research.
Jeff has presented his work at a number of different conferences including; the American Statistical Association, Immunogenicity for Protein-Based Therapeutics and EMCs Momentum conference.
Jeff earned a BS degree in Computational Mathematics from Michigan State University, East Lansing, Michigan.