Clinical Research Coordinator Jobs in Lauderhill,FL,US

Site Manager - Clinical Research (West Broward) Location: Lauderhill, FL (On-site) Shift: Monday-Friday | 9:00 AM - 5:00 PM Base Salary : $130K + Performance Bonuses Overview We are seeking a high-performing Site Manager to lead and optimize operations across our West Broward clinical research site. This role will oversee studies in neuroscience, women's health, and infectious disease, while also supporting the growth of emerging programs, including psychedelics research. This is a hands-on leadership role for someone who can stabilize operations, drive performance, and scale clinical trial delivery in a fast-paced environment. Key Responsibilities Oversee daily clinical site operations across multiple therapeutic areas Drive patient recruitment, screening, and enrollment performance Ensure compliance with FDA, GCP, and protocol guidelines Manage, mentor, and develop site staff (clinical and administrative) Monitor KPIs: enrollment, retention, data quality, and operational efficiency Collaborate with Sponsors, CROs, and internal leadership Optimize workflows and enhance patient experience Identify and resolve operational bottlenecks Ensure high-quality execution across all clinical trials Operational Scope Team Size: ~7 employees at site Reporting Structure: Reports to senior leadership; oversees site-level staff Active Trials: Multiple ongoing studies across therapeutic areas Systems: Experience with CTMS (Veeva preferred) is a plus Phase-Based Expectations Phase 1 (0-90 Days): Stabilize operations and improve site performance Strengthen recruitment funnel and enrollment conversion Evaluate team performance and implement accountability Phase 2 (90-180 Days): Scale operations and improve efficiency Identify process gaps and optimize workflows Phase 3 (180+ Days): Support leadership expansion and program growth initiatives Maintain operational excellence during scaling Qualifications 5+ years of clinical research experience, including site management Experience in CNS / psychiatric clinical trials Strong understanding of GCP, FDA regulations, and trial operations Proven ability to improve enrollment and site performance Experience managing cross-functional teams Strong leadership, organizational, and communication skills Preferred Qualifications Experience in neuroscience, women's health, or infectious disease trials Familiarity with Veeva CTMS or similar systems Background in scaling or optimizing clinical site operations Compensation & Benefits Competitive base salary: $130K Performance-based bonus (enrollment, retention, quality metrics) Additional incentive opportunities Full benefits package (health, dental, vision, 401k, PTO, etc.)