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Clinical Research Site Leader

2 months ago


Houston, Texas, United States The Las Olas Network LLC Full time

The Las Olas Network LLC is seeking a dedicated Clinical Site Director to manage and oversee multiple clinical trial locations.

This position is crucial for enhancing the operational efficiency of the research sites while ensuring that clinical research activities are executed in accordance with industry standards and regulations.

The responsibilities of the Clinical Site Director include:

  • Providing comprehensive leadership and management of the sites, focusing on performance improvement, patient safety, and adherence to protocols and regulatory requirements;
  • Collaborating with various departmental leaders, including those in Business Development, Patient Recruitment, Finance, and Quality Assurance, to align on project expectations and achieve study milestones;
  • Monitoring performance metrics and clinical trial systems to ensure optimal site and patient engagement, proper staffing, and timely updates on operational activities;
  • Managing resource allocation, site assignments, and the performance of study team members to ensure that deliverables are met, while identifying and mitigating risks to project timelines and quality;
  • Facilitating training sessions related to study protocols, data collection processes, and compliance with standard operating procedures;
  • Ensuring compliance with good clinical practice (GCP), FDA regulations, and organizational policies;
  • Supervising site staff and regularly evaluating compliance with study-specific processes, while developing corrective action plans as necessary.

The ideal candidate will possess a strong commitment to fostering high-performing teams and a desire to deepen their understanding of the business to enhance overall performance.

Minimum Qualifications: A Bachelor's degree along with a minimum of 8 years of experience in clinical research and at least 5 years in a management role, or an equivalent combination of education and experience. Experience in clinical research site management is highly desirable. Proficiency in both English and Spanish is preferred.

Required Skills:

  • Strong proficiency in computer applications, including Microsoft Office Suite and electronic health records;
  • Excellent organizational, time management, problem-solving, and project management abilities;
  • Exceptional written and verbal communication skills;
  • Strong interpersonal skills and the ability to work collaboratively with various stakeholders;
  • Capability to manage multiple tasks effectively and adapt to changing priorities;
  • Professional demeanor, respect for others, self-motivation, and a robust work ethic;
  • High level of integrity and reliability.