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Regional Site Manager

Remote / Online - Candidates ideally in
Bronx, Bonner County, Idaho, USA
Listing for: Proclinical
Full Time, Remote/Work from Home position
Listed on 2026-10-23
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 80000 - 120000 USD Yearly USD 80000.00 120000.00 YEAR
Job Description & How to Apply Below

Regional Site Manager
- Permanent
- Bronx, NY

Ready to lead high-performing clinical research sites and drive operational excellence across a growing region?

Proclinical is seeking a Regional Site Manager to oversee clinical research operations across multiple sites within an assigned region. The position requires a mix of remote work and travel to sites, with approximately 50% travel each month.

Primary Responsibilities:

The successful candidate will be involved in ensuring operational excellence, regulatory compliance, and high-quality research practices from study startup through closeout.

Skills & 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.
  • Bonus:
    Experience working with research-naive physicians and sites.
The Regional Site Manager's responsibilities will be:
  • 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.
Compensation:
  • $80 000 - $120 000/Annum
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