| Jill Chapman, BHSc, CCRA, worked in the clinical research industry for over ten years prior to joining ACRP in a staff position. Jill’s prior roles include in-house CRA, regional CRA, and Clinical Project Manager. She has worked in a phase 1 unit coordinating BA/BE studies on healthy volunteers, a large pharmaceutical company, a small biopharmaceutical company and a leading global CRO in various therapeutic areas and study phases. These prior positions enable Jill to approach member questions from various perspectives. In her current role, Jill assists members with their industry-related questions and serves as the staff liaison to the Regulatory Affairs Committee and the Professional Ethics Committee. Jill is entering her 10th year of being a Certified Clinical Research Associate. |