Clinical Research Operations Specialist

Oversee the end-to-end implementation and execution of assigned oncology studies across multiple Network sites, ensuring compliance with study protocols, timelines, and regulatory requirements. Act as a strategic liaison between pharma sponsors, contract research organizations (CROs), clinical sites, and internal teams to ensure alignment and execution of study objectives. Proactively identify operational risks and implement creative, timely solutions (SOPs, tools, and best practices) to optimize clinical trial workflow, patient recruitment, and data quality. Collaborate with regulatory, data, quality, and site teams to ensure compliance with applicable regulations and internal SOPs. Monitor trial progress, identify bottlenecks, and proactively address identified operational challenges. Participate in initiatives to establish best practices for optimizing patient enrollment in clinical trials.