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Regional Site Manager

Proclinical Bronx 22.10.2026 Déposer ma candidature
Company
Proclinical
Location
Bronx
Date
22.10.2026
Reference
372221

Lead High-Performing Clinical Research Sites

Drive operational excellence across a growing region by overseeing clinical research operations at multiple sites. This role combines remote work with regional travel, requiring approximately 50% travel each month to ensure high-quality research practices from study startup through closeout.

Primary Responsibilities

  • Supervise and support Clinical Research Coordinators (CRCs) across designated sites, including performance evaluations and guidance.
  • Recruit, interview, hire, and train CRCs on protocols, Good Clinical Practice (GCP), and regulatory requirements.
  • Manage study startup activities, including clinical trial agreements, budget preparation, IRB submissions, and site activation.
  • Track training completion for protocol updates and amendments.
  • Provide regular updates on study progress, enrollment, and data quality at each site.
  • Collaborate with study teams to resolve issues and ensure timelines are met.
  • Review and analyze study budgets and procedure costs to ensure cost-effective implementation.
  • Build relationships with local hospitals, laboratories, and vendors, coordinating operational readiness during startup.
  • Offer structured feedback to product and technology teams to refine platform features and workflows.

Skills and Requirements

  • Bachelor's degree in health sciences, clinical research, or a related field; advanced degree preferred.
  • Strong knowledge of GCP, FDA regulations, and clinical research operations.
  • Experience in site management roles, including hiring and supervising CRCs.
  • Familiarity with study startup processes, contracts, budgets, IRB submissions, and regulatory documentation.
  • Proven leadership and organizational skills to manage multiple studies, sites, and timelines.
  • Effective communication skills for collaboration with investigators, site staff, sponsors, CROs, and internal teams.
  • Ability to travel regionally as required.
  • Experience working with research-naive physicians and sites is a bonus.

Compensation

$80,000 - $120,000 per annum

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