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Regional Site Manager
Remote / Online - Candidates ideally in
Bronx, Bonner County, Idaho, USA
Listed on 2026-10-23
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
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.
- 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.
- $80 000 - $120 000/Annum
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