Patrick Kiser Email & Phone Number

Greater St. Louis Area

Chesterfield, Mo

IT Application Support and Enhancement Project Manager for a Fortune 500 company.

Swift provides clinical and health-related project management and data collection solutions for companies working within a variety of government-regulated environments, including those needing novel and innovative IT solutions. Swift provides services for entities requiring both clinic-based data management, and also large, multi-year field survey collection and recruitment efforts with populations from a variety of demographic and socioeconomic backgrounds.Responsibilities include bringing IT, data collection, and scientific experts to coordinate timelines, development, and implementation solutions, will ensure that roles and responsibilities are well defined, and work with clients and staff to help make each project a success. Services include: study start up, including clinical protocol development and obtaining regulatory approval; overseeing the development of computer systems life cycles for IT systems, including those utilizing mobile devices and external cloud-based environment; ensuring that regulatory requirements are implemented successfully, including those required by the Food And Drug administration (including 21 CFR Part 11), Health Insurance Portability and Accountability Act, and the Federal Information Security Management Act; tracking study progress; tracing respondents lost to follow up; and addressing client needs and concerns.

Greater St. Louis Area

Senior IT Project Manager supporting the implementation of ServiceNow at a Fortune 500 company.

St. Louis, Mo

For 20 years, I managed projects collecting and processing health data within a variety of government-regulated environments. I was responsible for delivering milestones for several multi-million dollar projects, including clinical trial contracts for the Department of Defense and commercial clients, and large, multi-year field survey collection and recruitment efforts with populations from a variety of demographic and socioeconomic backgrounds.In addition to ensuring that these studies were conducted on time and within budget, I have worked with IT, data management, and scientific experts to ensure that staff understood their roles and responsibilities to help make each project a success. Tasks included: study start up, including clinical protocol development and obtaining regulatory approval; overseeing the development of computer systems life cycles for IT systems, including those utilizing mobile devices and external cloud-based environment; ensuring that regulatory requirements were implemented successfully, including those required by the Food And Drug administration (including 21 CFR Part 11), Health Insurance Portability and Accountability Act, and the Federal Information Security Management Act; tracking study progress; and addressing client needs and concerns.