Regional Site Manager

Proclinical; New York (NY); Hybrid; USD 80,000 - 120,000; Full time

Job summary

Proclinical is seeking a Regional Site Manager to oversee clinical research operations across multiple sites within an assigned region. The role blends remote work with on-site travel, averaging about 50% travel each month.

You will supervise CRCs, ensure regulatory compliance, and lead startup activities from contract through activation, while coordinating with sponsors, CROs, and internal teams to meet timelines and budgets.

Qualifications

• Bachelor's degree in health sciences, clinical research, or related field; advanced degree preferred.
• GCP knowledge, 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 for collaboration with investigators, site staff, sponsors, CROs, and internal teams.
• Ability to travel regionally as required.
• Bonus: experience with research-naive physicians and sites.

Responsibilities

• Supervise and support Clinical Research Coordinators (CRCs) across designated sites, including performance evaluations and guidance.
• Recruit, interview, hire, and train CRCs on protocols, 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

GCP

FDA regulations

Site management

Study startup

IRB submissions

Budgets

Leadership

Communication

Travel

Education

Bachelor's degree in health sciences

Advanced degree preferred

Job description

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