Site Director

Overview

• Lead and oversee the operations of a clinical research site, ensuring excellence in study execution and regulatory compliance.
• Drive strategic initiatives to enhance site performance and achieve organizational goals effectively.
• Collaborate with cross-functional teams to ensure quality data collection and patient safety throughout studies.
• Manage resource allocation, staff development, and operational deliverables to optimize efficiency and outcomes.
• Provide leadership in training, protocol adherence, and clinical operations management to ensure success.
• Implement innovative solutions to mitigate risks and ensure study success and compliance.
• Foster a culture of excellence, collaboration, and continuous improvement within the site.
• Ensure compliance with industry standards, including ICH, GCP, and FDA guidelines.

Key Responsibilities & Duties

• Oversee all aspects of site operations, including staffing, resource management, and performance evaluations.
• Coordinate with investigators and teams to ensure patient safety and study success.
• Monitor site activities using dashboards and systems to maintain data accuracy and integrity.
• Conduct training sessions on protocols, SOPs, and clinical research practices.
• Develop and implement corrective action plans to address operational risks effectively.
• Ensure adherence to regulatory requirements and company policies at all levels.
• Collaborate with department leaders to meet study budgets and timelines efficiently.
• Drive operational efficiencies and foster a collaborative and productive team environment.

Job Requirements

• Bachelor’s degree in Science with 5+ years of clinical research experience required.
• Minimum 2 years of experience managing clinical research sites or equivalent leadership roles.
• Proficiency in Microsoft Office, electronic health records, and web-based tools essential.
• Strong organizational, project management, and strategic thinking skills are critical.
• Excellent communication and interpersonal abilities to lead and collaborate effectively.
• Experience in staff management, performance evaluations, and team development required.
• Knowledge of ICH, GCP, and FDA guidelines is essential for compliance.
• Bilingual proficiency in English and Spanish is advantageous but not mandatory.