Clinical Study Manager

Lead end-to-end execution of clinical studies supporting feasibility, pivotal, and post-market development programs. Own study startup through close-out, including timelines, enrollment planning, monitoring plan implementation, risk mitigation, and site engagement. Partner with Clinical Affairs and cross-functional teams (Regulatory, Data Management, Biostatistics) to ensure compliant, high-quality data outcomes. Manage CROs, vendors, and study partners, and support audits, inspections, and clinical documentation submissions.