Experience

PharmaSUG

• United States
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Executive Committee Member

  • Jun 2014 - Present

  PharmaSUG 2023 Academic co-chair PharmaSUG 2023 Academic co-chair


IQVIA
• United States
• Hospitals and Health Care
• 700 & Above Employee
• Senior Standards Engineer

  • Jan 2022 - Present

Clinical Solutions Group (CSG, Inc.)
• Senior Standards Engineer

  • Oct 2019 - Dec 2021


Syneos Health Clinical Solutions (Previously INC Research/inVentiv Health)

• Senior Engineer

  • Jan 2018 - Oct 2019

  Syneos Health™ is the only fully integrated biopharmaceutical solutions organization. Our company, including a Contract Research Organization (CRO) and Contract Commercial Organization (CCO), is purpose-built to accelerate customer performance to address modern market realities. Created through the merger of two industry leading companies — INC Research and inVentiv Health — we bring together more than 21,000 clinical and commercial minds with the ability to support customers in more than 110 countries. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients. In short, we are shortening the distance from lab to life™. Show less


inVentiv Health Clinical
• United States
• Pharmaceutical Manufacturing
• 500 - 600 Employee
• Principal Statistical Programmer

  • Sep 2014 - Jan 2018


Ephicacy Lifescience Analytics

• Principal programmer

  • Apr 2011 - Aug 2014

  April 2014 - August 2014 Theravance - Lead programmer on SDTM & ADaM datasets and TLG's April 2011 - April 2014 GlaxoSmkithKline - Principal Programmer on SDTM & ADaM datasets and displays April 2014 - August 2014 Theravance - Lead programmer on SDTM & ADaM datasets and TLG's April 2011 - April 2014 GlaxoSmkithKline - Principal Programmer on SDTM & ADaM datasets and displays



Village of Maple Bluff

• Village Trustee

  • May 2010 - Sep 2013

  Elected Official Elected Official



Covance

• United States
• Research Services
• 700 & Above Employee

• Expert Programmer/Analyst (Programmer IV)

  • May 2009 - Apr 2011

  • Lead for the mapping of CRFs to CDISC/SDTM datasets for all clinical phases.• Primary for implementing CDISC/ADaM datasets for Table, Listing, and Figure production.• Direct the creation of CDISC compliant CRFs, using CDASH recommendations to be used by the clinical research units.• Maintain the set of SAS macros that create the DEFINE.XML document for FDA submission.• Offer technical leadership to the data management, programming and biostatistics groups in the use of SAS.• Give guidance, mentoring and training to other programmers.• Provide support programming for the production of tables, listings, graphs, and analyses related to clinical studies.• Transfer data to and from clients in both production and developmental roles, including designing, coding, testing, and implementing project work using SAS.• Improve CDISC dataset creation by 30% using Six Sigma (“improve phase”). Show less

• Senior Programmer/Analyst (Programmer III)

  • May 2004 - May 2009

  • Lead for the mapping of CRFs to CDISC/SDTM datasets for Phase 1.• Create the set of SAS macros that creates the DEFINE.XML document for FDA submission.• Provide technical support to the data management group in the use of Oracle Clinical and to the programming and biostatistics groups in the use of SAS.• Transfer data to and from clients in both production and developmental roles, including designing, coding, testing, and implementing project work using SAS.• Serve as the liaison between data management, programming, and biostatistics.• Supply programming for the production of tables, listings, graphs, and analyses related to clinical studies.• Create and deliver datasets to clients.• Mentor other programmers and develops departmental standard processes.• Improve CDISC dataset creation by 30% using Six Sigma (“implementation phase”). Show less

• Staff Associate (Programmer II)

  • May 2000 - May 2004

  • Produce report tables for studies, as assigned, including production of programs in SAS, to meet client specifications.• Develop mock up tables for report and analysis plans.• Lead for data transfer to and from clients in both production and developmental roles though design, code, tests, and implementing project work using SAS.• Interact with clients on programming matters, performing special programming in response to unscheduled requests and support for the SAS applications and/or Oracle application.• Maintain SAS and/or the data entry specifications.• Assist with data entry database comparisons and database audits.• Develop programmable edit checks to assist in data review.• Support in maintaining ISO 9001 registration through 2001.• Perform other related duties as assigned. Show less

• Staff Associate (Developer)

  • May 1998 - May 2000

  • Responsible for the production of report tables for studies, as assigned, including production of programs in SAS, to meet client specifications.• Involvement in data transfer to and from clients in both production and developmental roles.• Design, code, test, and implement project work in SAS.• Assist with the backup of network servers.• Responsible for data entry database comparisons and database audits.• Provide support for Oracle and Data Entry applications and develop mock-up tables for report and analysis plans.• Assist in maintaining ISO 9001 registration. Show less



University of Wisconsin Milwaukee

• United States
• Higher Education
• 700 & Above Employee

• SAS Programmer

  • Sep 1996 - Dec 1997

  • Create SAS Web pages • Generate Oracle Data Base using SAS • Worked on a billing system for telephone use using SAS • Create SAS Web pages • Generate Oracle Data Base using SAS • Worked on a billing system for telephone use using SAS