• 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. • Review and provide input on essential study documents (e.g., protocols, informed consents, site training materials). • Oversee trial-specific training for internal stakeholders and site teams. • Responsible for operational input and oversight in designing, planning, initiating and completing clinical trials across assigned disease teams. • Lead clinical study and cross functional team to make key decisions related to strategy and issue resolution. • Participate in initiatives to establish best practices for optimizing patient enrollment in clinical trials. • Collaborate with stakeholders to develop and implement trial specific training programs. • Innovate and implement novel patient enrollment strategies to maximize clinical trial participation. • Identify and integrate new tools, workflows, and methodologies to improve protocol implementation and patient enrollment processes. • Perform additional duties and responsibilities as required.