Site Director

Overview

• Lead operational performance and ensure compliance with clinical research guidelines and regulations.
• Provide on-site oversight for clinical research activities, ensuring quality and efficiency.
• Collaborate with department leaders to meet study milestones and deliver quality data.
• Oversee site staff, ensuring proper training and adherence to protocols.
• Manage site operations, including staffing, payroll, and resource allocation.
• Develop and implement corrective action plans to address emerging risks.
• Ensure patient safety and compliance with regulatory requirements.
• Participate in strategic planning and management meetings.

Key Responsibilities & Duties

• Drive site performance and enhance operational efficiencies.
• Coordinate with department leaders to achieve study objectives.
• Monitor dashboards and systems to oversee site activities and performance.
• Ensure compliance with SOPs, GCP, FDA regulations, and company policies.
• Manage site staff, including hiring, training, and performance evaluations.
• Collaborate with investigators to ensure patient safety and study goals.
• Identify risks and implement solutions to maintain study deliverables.
• Prepare and present reports in management meetings.

Job Requirements

• Bachelor’s degree in science or equivalent combination of education and experience.
• Minimum of 7 years in clinical research, with 2 years in management.
• Proficiency in Microsoft applications and electronic health records.
• Strong organizational, time management, and problem-solving skills.
• Excellent communication and interpersonal abilities.
• Experience managing site operations and achieving KPIs.
• Ability to handle sensitive information confidentially and professionally.
• Bilingual proficiency in English and Spanish is a plus.