Members of our senior management team hold an average of 25+ years experience in clinical research. Together with PharPoint’s founders, they lead our teams in anticipating challenges, providing quality solutions, and staying ahead of clinical trial deadlines.
Jayme Swinson, MS Vice President, Operations
Years of Industry Experience: 20+ years
Expertise includes: Database programming, data standardization, data warehousing
Education: MS in Mathematics, University of North Carolina at Wilmington
Additional Experience: As one of the original members at PharPoint, Mr. Swinson established and led the programming department, defining and refining standard processes across functional areas. He’s supported trials across a range of therapeutic areas from Phase 1 to Phase 4 as well as patient registries.
Expertise includes: Data management; biometric strategy and oversight; EDC; managing/providing oversight for global, multilingual studies
Education: BS from Appalachian State University
Additional Experience: Ms. Hawkins has served on EDC steering committees within several companies, helping organizations decide on and implement new data capture technologies. In addition to her work at PharPoint, she has served on a committee for the Society of Clinical Data Management, a non-profit dedicated to the advancement of clinical data management.
Paul Johnson Executive Director, Strategy Development
Years of Industry Experience: 30+ years in health care
Education: BS, Biology/Natural Science from Midland University
Additional Experience: Mr. Johnson has participated in numerous studies across a breadth of therapeutic areas. This includes experience managing, providing oversight for, and rescuing oncology studies; experience evaluating antiretroviral therapies; and extensive Phase 1 experience in normal, healthy volunteers in multiple indications.
Stacey Smith Will, CCRA Senior Director, Clinical Operations
Years of Industry Experience: 25+ years
Expertise includes: Risk mitigation, leadership development, process innovation, clinical site management and monitoring
Education: BA Business Management, North Carolina State University; BA Speech-Communication, North Carolina State University; Certified Clinical Research Associate (CCRA)
Additional Experience: Ms. Will has a highly diverse therapeutic background including autoimmune disorders, infectious disease including COVID, vaccines, rare disease, endocrinology, gastroenterology, & oncology. She is passionate about improving lives through quality delivery of clinical trials.
Karisa Satterly Director, Business Development
Years of Industry Experience: 10+ years
Expertise includes: Initiatives for growth and diversification of pipeline of work in the clinical research industry
Education: BBA from Texas A&M University
Additional Experience: Prior to PharPoint, Ms. Satterly held various roles of increasing responsibility in the data management industry, including positions in business analytics, marketing, business development, and account management.
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