Site Director Overview • The Site Director oversees clinical research site operations to ensure compliance with industry standards and organizational policies. • Responsible for driving operational performance, enhancing efficiencies, and maintaining high standards of patient safety and protocol adherence. • Collaborates with cross-functional teams to meet study milestones, budgets, and deliver quality data to sponsors. • Ensures proper staff coverage and timely execution of operational aspects through performance dashboards and clinical trial systems. • Provides training on protocols, SOPs, clinical plans, and guidelines to ensure adherence to regulatory standards. • Manages site staff, including hiring, performance appraisals, and career coaching to maintain effective operations. • Collaborates with investigators to ensure patient safety and achieve client goals within established timelines. • Employs strategic thinking to propose and implement risk mitigations for site operations. • Participates in management meetings and contributes to organizational strategy and development. Site Director Key Responsibilities & Duties • Lead site management efforts focusing on performance, efficiency, and compliance with GCP and FDA guidelines. • Coordinate with department leaders to meet study milestones, budgets, and deliverables. • Monitor site and patient activities using dashboards to ensure operational efficiency and compliance. • Oversee resource allocation, site assignments, and team performance to meet study objectives. • Conduct training sessions on protocols, SOPs, and clinical guidelines to ensure adherence to standards. • Manage site staff, including recruitment, performance reviews, and training for optimal operations. • Develop corrective action plans to address compliance and operational risks. • Collaborate with investigators to ensure patient safety and study success. • Participate in organizational meetings and contribute to strategic planning and execution. Site Director Job Requirements • Bachelor’s degree in Science or equivalent education and experience in clinical research. • Minimum of 7 years of clinical research experience, with 2 years in management roles. • Proficiency in Microsoft applications, electronic health records, and web-based tools. • Strong organizational, time management, and problem-solving skills to meet deadlines. • Excellent communication and interpersonal skills for effective collaboration. • Experience in site management, including KPI tracking, hiring, and performance reviews. • Ability to handle sensitive information confidentially and professionally. • Bilingual proficiency in English and Spanish is a plus. • Willingness to relocate and adapt to organizational needs.