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Regional Site Manager

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Remote

Regional Site Manager

Proclinical Staffing

Regional Site Manager

Skills

Google Cloud PlatformBudgetingComplianceRegulatory Compliance

6 days ago

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Important information


Contract type:

Permanent

Salary:

$80,000 – $120,000 / year

Location:

New York, NY, USA

Work mode:

Remote

Published on:

21 October 2026

What they need


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

If you are having difficulty in applying or if you have any questions, please contact Alex Kelly at [email protected].

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy

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