Site Supervisor/Study Project Manager

Segal Trials

Florida

Presencial

USD 80.000 - 100.000

Jornada completa

14 días+

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Descripción de la vacante

Segal Trials is seeking a Site Manager to oversee operations at clinical research sites in West Broward. The role requires a blend of leadership and hands-on project management to optimize site performance and ensure compliance with regulatory standards.

The ideal candidate will have experience in recruitment, staff management, and operational excellence within clinical trials. Key responsibilities include managing daily site operations, driving participant recruitment, and serving as the primary contact for study sponsors.

Formación

  • Experience managing clinical research sites, especially in neuroscience or psychiatry.
  • Strong understanding of GCP, FDA regulations, and study protocols.
  • Proven track record in recruitment and staff management.

Responsabilidades

  • Manage daily operations and performance at research sites.
  • Drive recruitment, screening, and retention of study participants.
  • Ensure compliance with regulatory standards and protocols.

Conocimientos

Leadership
Regulatory Compliance
Study Project Management
Site Operations Management
Recruitment and Enrollment

Descripción del empleo

The Site Manager will oversee operations across West Broward clinical research sites, supporting both neuroscience and psychedelics programs. This role blends site leadership with hands‑on study project management, with responsibility for stabilizing, optimizing, and scaling site performance while helping build future program leadership structures.

Role Summary

Responsible for overall site performance, including recruitment, enrollment, staff management, regulatory compliance, and study execution. Serves as both operational leader and Study Project Manager for high‑priority trials.

Key Responsibilities
  • Oversee daily site operations and staff performance
  • Drive recruitment, screening, enrollment, and retention
  • Ensure compliance with GCP, FDA, and protocol requirements
  • Serve as primary contact for sponsors, CROs, and vendors
  • Manage study timelines, deliverables, and issue resolution
  • Monitor KPIs including enrollment, retention, quality, and profitability
  • Maintain CTMS and data entry compliance
  • Train, mentor, and develop research staff
  • Conduct performance evaluations and manage staffing needs
  • Collaborate cross‑functionally with HR, Recruitment, Finance, and Marketing
  • Improve workflows and operational systems
Phase-Based Expectations
0–90 Days
  • Stabilize operations and improve recruitment funnel
  • Assess team performance and implement accountability
  • Ensure protocol and regulatory compliance
90–180 Days
  • Scale enrollment and site efficiency
  • Identify bottlenecks and optimize processes
  • Define structure for future program leadership
180+ Days
  • Support hiring and onboarding of program leadership
  • Maintain operational excellence during transition
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