Site Director

Overview

• Lead a high-performing clinical research site, ensuring operational excellence and regulatory compliance.
• Drive strategic initiatives to enhance site performance and achieve study milestones.
• Collaborate with cross-functional teams to deliver quality data and patient safety.
• Oversee resource allocation, staff management, and operational deliverables.
• Provide leadership in training, protocol adherence, and clinical operations.
• Implement strategic solutions to mitigate risks and ensure study success.
• Foster a culture of excellence and continuous improvement within the site.
• Ensure compliance with industry standards, including ICH, GCP, and FDA guidelines.

Key Responsibilities & Duties

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

Job Requirements

• Bachelor’s degree in Science with 5+ years of clinical research experience.
• Minimum 2 years of experience managing clinical research sites.
• Proficiency in Microsoft Office, electronic health records, and web-based tools.
• Strong organizational, project management, and strategic thinking skills.
• Excellent communication and interpersonal abilities.
• Experience in staff management and performance evaluations.
• Knowledge of ICH, GCP, and FDA guidelines is essential.
• Bilingual proficiency in English and Spanish is advantageous.