Site Director

Sci-Rec

Miami (FL)

On-site

USD 120,000 - 160,000

Full time

6 days ago
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Job summary

Sci-Rec in South Florida seeks a hands-on Clinical Research Site Manager to lead a busy site and a growing neuroscience/psychedelic research program. You will oversee day-to-day operations, ensure high-quality data, and manage a large team across multiple Phase I–IV trials.

You will report to Clinical Operations and the Medical Director, coaching staff, optimizing processes, and driving site profitability while maintaining rigorous regulatory standards.

Qualifications

  • 6+ years in clinical research with leadership/management experience.
  • Experience running a site with multiple Phase I–IV trials and 30+ staff.
  • Strong knowledge of ICH-GCP, FDA regs, HIPAA; CAPA, auditing, QA.
  • Proficiency with CTMS, EDC and eRegulatory systems.
  • Hands-on, data-driven leader with clear communication.
  • Bachelor’s degree in a related field preferred

Responsibilities

  • Lead site operations across Phase I-IV trials: recruitment, screening, enrollment, retention, visit completion and data quality.
  • Coach and develop CRCs, Lead CRCs, regulatory coordinators, recruitment staff and research assistants.
  • Act as Study Project Manager from startup to closeout on high-priority trials.
  • Track KPIs, identify barriers early and drive CAPAs and workflow improvements.
  • Maintain FDA/ICH-GCP/HIPAA compliance with Regulatory and Compliance team.
  • Serve as primary sponsor/CRO contact and manage staffing and budgets with leadership.
  • Drive site growth and develop next-gen operational leaders.

Skills

Leadership
Communication
Data-driven mindset
Strategic planning

Education

Bachelor's degree in a related field

Tools

CTMS
EDC
eRegulatory systems

Job description

Clinical Research Site Manager | South Florida

An established, founder-owned clinical research organisation with 20 years of organic growth is looking for a hands-on site leader to run a busy site in South Florida. You'll lead a large team, 16-18 active trials at a time, and a growing neuroscience and psychedelic research programme.

The role

You'll own the day-to-day performance of the site: strategy and operations, and the occasional shift on the floor. You'll be a leader who sets direction and also steps in as backup when the team is busy. You'll report into Clinical Operations and the Medical Director.

What you'll do
  • Lead site operations across Phase I-IV trials: recruitment, screening, enrollment, retention, visit completion and data quality
  • Manage and develop CRCs, Lead CRCs, regulatory coordinators, recruitment staff and research assistants through coaching, training and performance reviews
  • Act as Study Project Manager on high-priority trials, from startup through closeout
  • Track KPIs, spot barriers early and drive CAPAs and workflow improvements
  • Keep the site inspection-ready and compliant with FDA, ICH-GCP, HIPAA and ALCOA+ standards, working closely with the Regulatory and Compliance team
  • Be a primary contact for sponsors and CROs
  • Work with Finance and leadership on staffing, budgets and site profitability
  • Support site growth and develop the next generation of operational leaders
What you'll bring
  • 6+ years in clinical research, including 4+ years in leadership or management
  • Experience running a clinical research site with multiple Phase I-IV trials, and managing a team of 30+
  • Strong knowledge of ICH-GCP, FDA regulations and HIPAA, and of CAPA, auditing and quality management
  • Proficiency with CTMS, EDC and eRegulatory systems
  • A hands-on, collaborative leadership style, a data-driven mindset and strong communication
  • Bachelor's degree in a related field preferred (equivalent experience considered)
Nice to have
  • Experience in CNS, neuroscience, psychiatric or psychedelic research
  • CCRC or CCRP certification
Why this role
  • Lead a standalone site with real autonomy and influence
  • Join a stable, founder-owned organisation with 20 years of growth behind it
  • Help shape a growing neuroscience and psychedelic research programme
  • Work with a close-knit, experienced team
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