Wendy Cline

Wendy Cline is an experienced project manager specializing in study start-up processes within the clinical research industry. Currently serving as a Study Start-Up Project Manager at Pfizer since January 2022, Wendy’s previous roles include similar positions at ExecuPharm and Medpace, as well as a Senior Regulatory Submission Manager role at Medpace. Wendy has extensive experience at Syneos Health and inVentiv Health Clinical, where positions included Senior Study Start-Up Project Lead and Global Study Start-Up Manager. Early career roles included various positions at PPD and Duke Clinical Research Institute, contributing to expertise in clinical submission and site start-up processes since starting in the field with Unifour Medical Research Associates.