Page Executive
- Provide strategic and scientific oversight for the planning and execution of early-stage clinical trials in neurodegeneration.
- Design and implement clinical development plans, including study protocols, timelines, and endpoints aligned with regulatory and commercial goals.
- Serve as the clinical initiator for interactions with regulatory authorities (FDA, IRBs) for early development programs.
- Oversee clinical trial site selection, investigator engagement, and vendor management (., CROs, biometrics, medical monitoring).
- Interpret clinical trial data and ensure timely, high-quality reporting.
- Work with preclinical, translational, regulatory, and CMC teams to do IND filings and study readiness.
- Represent the company in key scientific, clinical, and regulatory discussions.
- Build and mentor a high-performing clinical development team as the organization scales.