Senior Manager Clinical Trial Program (Stroke Institute)

Seeking a person highly experienced in human research studies, with the ability to train research staff on how to coordinate and manage clinical trials. This is a working leadership role in the Institute for Stroke and Cerebrovascular Disease with the expectations that the person will have good knowledge on research compliance, has experience in audits for clinical trial studies, and is capable of leading internal audits. Experience with CAPA (Corrective and Preventative Action) plans and being able to oversee 8 research staff with day-to-day activities. This role will be expected to assist with writing research protocols as well as overseeing a program for peer reviewed pilot studies. This position will not be much involved in subject recruiting or enrollment but will be managing and training the staff on site development, enrollment of human subjects and clinical trial monitoring. This role is focused on management of multiple studies with the expectation to learn and know the SOP’s for each study. This is not a research administrator (pre/post award) position. Confidence, great presentation skills, and strong collaborative skills are also required. Experience writing research protocols is also a great asset.