Director, Site Management

Key Responsibilities

• Oversee day-to-day operations of multiple clinical research sites, apply and facilitate governance management of sites
• Monitor and drive performance metrics including enrollment, retention, protocol adherence, and visit compliance
• Own and manage site-level P&Ls; ensure financial targets are met or exceeded
• Partner with Finance to develop budgets, forecasts, and cost control strategies
• Identify opportunities for revenue growth and operational efficiency
• Ensure timely and high-quality execution of all aspects of clinical trials across all sites
• Own successful application of solutions, oversight and where applicable KPIs to ensure all sites within responsibility exceed recruitment targets for every study
• Collaborate with study sponsors, CROs, and internal stakeholders to meet study timelines and expectations
• Serve as a key liaison between site operations, corporate departments (e.g., HR, Finance, Regulatory), and executive leadership

Qualifications

• Bachelor’s degree in life sciences, healthcare, or related field (master’s preferred)
• 8+ years of experience in clinical research, with 3+ years in multi-site or regional leadership
• Strong knowledge of clinical trial operations, regulatory requirements, and site management
• Proven experience managing P&Ls and driving financial performance
• Excellent leadership, communication, and organizational skills
• Willingness to travel extensively (up to 75%)