The CRRS B will play a key role in coordinating trial start-up activities from feasibility assessment through site activation, working closely with PNTC Project and Business Managers, investigators, study teams, institutional offices, sponsors, and contract research organizations (CROs). Responsibilities will include coordinating and tracking regulatory and ancillary submissions, essential study documentation, and other startup requirements to support efficient and timely study activation. Following activation, the CRRS B will collaborate with study teams to provide ongoing regulatory support, including protocol amendments, continuing reviews, reportable events, regulatory documentation, maintenance of complete and inspection-ready study files, and coordination of monitoring visits and audits.
The ideal candidate will be highly motivated, organized, and detail-oriented, with a proactive and collaborative approach and the ability to plan and manage multiple priorities and deadlines in a fast-paced clinical research environment. Prior experience with regulatory/ethics boards/ancillary submissions and reviews, industry-sponsored early-phase clinical trials, and/or gene therapy research is strongly preferred.