Clinical Research Site Director

Lead and oversee clinical research site operations across multiple locations, driving performance, protocol/GCP/ICH adherence, and timely trial delivery. Coordinate with Business Development, Patient Recruitment, Finance, Contracts, and Quality to achieve site activation and enrollment milestones within budget while maintaining data integrity and regulatory compliance. Manage staff allocations, training on protocols, CRFs, and SOPs; develop corrective action plans; ensure patient safety and data quality; supervise payroll and onboarding; collaborate with investigators to meet client goals and timelines; and contribute strategic problem-solving to mitigate risks. Strong leadership, organizational, and communication skills, with emphasis on HIPAA compliance and bilingual (English/Spanish) capability preferred.