Remote Clinical Operations Lead - Multi-Site

SiteBridge Research

Chapel Hill (NC)

On-site

USD 95,000 - 135,000

Full time

14 days+
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Job summary

SiteBridge Research Inc. is seeking an experienced Clinical Operations Manager to provide oversight of CRCs and site staff across our network. You will ensure study readiness, protocol adherence, and performance against KPIs while maintaining FDA/ICH GCP compliance and SOP alignment.

You will manage staffing plans, support start-up and close-out activities, and collaborate with recruitment, budget, and finance teams to drive site success. Remote work with up to 30% travel is required.

Qualifications

  • Bachelor's degree or higher with clinical research experience.
  • Minimum 4 years in clinical research; CRC/CRA/site lead experience required.
  • Minimum 2 years supervising CRCs or site staff.
  • Spanish-speaking applicants encouraged.
  • Strong knowledge of FDA & ICH GCP regulations.
  • Experience with eSource, eRegulatory and CTMS preferred.

Responsibilities

  • Provide day-to-day oversight of CRCs and site staff across multiple sites; ensure readiness and protocol compliance.
  • Own site and CRC performance against KPIs; identify gaps and trigger corrective actions.
  • Drive enrollment plans to meet recruitment goals for each study.
  • Oversee CRC hiring, onboarding, training, and performance management.
  • Support start-up, maintenance, and close-out activities across sites.
  • Partner with recruitment, budget, and finance teams to drive site success.
  • Ensure SOP compliance and timely regulatory submissions; coordinate audits as needed.
  • Travel up to 30% for site development and operational needs.

Skills

Leadership
Project management
Communication
Bilingual Spanish
FDA & ICH GCP knowledge
eSource/eRegulatory/CTMS

Education

Bachelor's degree

Tools

eSource
eRegulatory
CTMS
SOPs

Job description

SiteBridge Research Inc. is seeking an experienced Clinical Operations Manager to provide oversight of CRCs and site staff across our network. You will ensure study readiness, protocol adherence, and performance against KPIs while maintaining FDA/ICH GCP compliance and SOP alignment.

You will manage staffing plans, support start-up and close-out activities, and collaborate with recruitment, budget, and finance teams to drive site success. Remote work with up to 30% travel is required.

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