• Provide operational oversight and coordination for Pediatric Acute Leukemia clinical trials. • Serve as the primary liaison between the pharmaceutical clinical research team and CROs. • Ensure trials are executed efficiently, on budget, and in compliance with regulatory standards. • Lead cross-functional teams to deliver high-quality studies evaluating safety and efficacy of pharmaceuticals. • Monitor study activities for compliance with protocols and regulatory requirements. • Identify potential delays or out-of-scope work and implement mitigations. • Oversee study documentation, including case report forms, drug records, and regulatory filings. • Maintain regular communication with sponsors and internal teams. • Develop realistic budgets and timelines.