Key Responsibilities: Travel to assigned research sites to manage day to day study operations including patient recruitment, screening, enrollment, and follow up visits Educate and support site personnel on study procedures, expectations, and compliance requirements Coordinate site opening activities to ensure new sites are prepared for study launch Support early enrollment efforts by guiding sites through startup tasks and recruitment expectations Independently manage travel logistics including scheduling, travel documentation, and proactive communication with site stakeholders Maintain audit and inspection readiness and support sites during monitoring visits and regulatory reviews. Skills: Strong understanding of clinical trial operations from startup through close out Extensive knowledge of GCP, GDP, and ALCOA+ principles Experience with EDC platforms such as Medidata Rave, Veeva, or Oracle and CTMS systems Ability to work independently in fast paced, travel intensive environments Strong problem solving, organizational, and attention to detail skills Excellent communication and relationship building skills with sponsors, CROs, monitors, site staff, and participants Ability to manage multiple projects and meet deadlines in a multi site environment.