Clinical Site Director

Green Key Resources; Orlando (FL); On-site; USD 120,000 - 180,000; Full time

Job summary

Green Key Resources is seeking an experienced Clinical Site Director to lead day-to-day operations at a clinical research site. You will oversee site staff, study execution, patient safety, regulatory compliance, and overall operational efficiency to meet enrollment, timeline, quality, and budget expectations.

Key responsibilities include leading site operations, ensuring compliance with ICH/GCP and FDA regulations, monitoring performance and enrollment, developing staff, and coordinating with

Qualifications

• Bachelor’s degree and 5+ years of clinical research experience.
• 2+ years of clinical research site management experience required.
• Strong leadership, organizational, communication, problem-solving, and project management skills.
• Working knowledge of GCP, FDA regulations, HIPAA, and clinical research site operations.

Responsibilities

• Lead overall site operations, performance, staffing, and clinical research activities.
• Ensure compliance with ICH/GCP, FDA regulations, SOPs, and study protocols.
• Monitor study performance, enrollment, patient activity, timelines, and quality metrics.
• Manage and develop site staff, including hiring, training, performance management, and coaching.
• Partner with Business Development, Patient Recruitment, Finance, Contracts, Quality, and investigators to achieve study milestones.
• Identify operational risks and implement corrective action and mitigation plans.
• Ensure appropriate site resourcing and staff coverage across assigned studies.
• Support protocol-specific training, CRF completion, and study documentation.
• Collaborate with investigators to ensure patient safety and successful study execution.

Skills

Leadership

Organizational skills

Communication

Problem-solving

Project management

Team development

Education

Bachelor’s degree

Job description

We8re seeking an experienced Clinical Site Director to lead day-to-day operations and drive performance at a clinical research site. This individual will oversee site staff, study execution, patient safety, regulatory compliance, and overall operational efficiency while ensuring studies meet enrollment, timeline, quality, and budget expectations.

Key Responsibilities:

• Lead overall site operations, performance, staffing, and clinical research activities
• Ensure compliance with ICH/GCP, FDA regulations, SOPs, and study protocols
• Monitor study performance, enrollment, patient activity, timelines, and quality metrics
• Manage and develop site staff, including hiring, training, performance management, and coaching
• Partner with Business Development, Patient Recruitment, Finance, Contracts, Quality, and investigators to achieve study milestones
• Identify operational risks and implement corrective action and mitigation plans
• Ensure appropriate site resourcing and staff coverage across assigned studies
• Support protocol-specific training, CRF completion, and study documentation
• Collaborate with investigators to ensure patient safety and successful study execution

Qualifications:

• Bachelor’s degree and 5+ years of clinical research experience, or equivalent combination of education and experience
• 2+ years of clinical research site management experience required
• Strong leadership, organizational, communication, problem-solving, and project management skills
• Working knowledge of GCP, FDA regulations, HIPAA, and clinical research site operations

This is an excellent opportunity for an experienced clinical research leader who enjoys building strong teams, improving site performance, and ensuring high-quality study execution.