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Director Site Operations

Green Life Science

Manchester

On-site

GBP 60,000 - 80,000

Full time

Yesterday
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Job summary

A healthcare organization in clinical research is seeking a Senior Manager to oversee multi-site partnerships for clinical research. The ideal candidate will have a Bachelor's degree in a science-related field and over six years of experience in clinical research, including three years in a leadership role. Responsibilities include managing partnerships, ensuring compliance with regulations, and optimizing site operations. This role includes a focus on building relationships with site leaders and financial oversight.

Qualifications

  • Bachelor’s degree or equivalent in a science-related field.
  • 6+ years of clinical research experience, with 3+ years in a leadership role.
  • Strong knowledge of site operations and trial delivery.

Responsibilities

  • Own and manage clinical research site partnerships end to end.
  • Lead site onboarding and ongoing operational optimization.
  • Ensure compliance with ICH-GCP and regulatory standards.

Skills

Clinical research management
Leadership
Site operations expertise
Regulatory compliance
KPI monitoring

Education

Bachelor’s degree in a science-related field

Tools

CTMS platforms
Job description

A healthcare organization within the clinical research sector is seeking a Senior Manager to lead the operational and strategic oversight of partnered research sites. This role is responsible for ensuring high-quality execution, regulatory compliance, and strong performance across a multi-site research environment.

Responsibilities
  • Own and manage clinical research site partnerships end to end
  • Lead site onboarding and ongoing operational optimization
  • Build strong relationships with site leaders, sponsors, and internal teams
  • Oversee budgets, contracts, and financial performance
  • Ensure compliance with ICH-GCP, regulations, and audit readiness
  • Monitor KPIs and drive operational improvements
  • Line manage and develop site-based teams
  • Oversee use of CTMS, eConsent, eSource, and related systems
Qualifications
  • Bachelor’s degree in a science-related field or equivalent experience
  • 6+ years of clinical research experience; 3+ years in leadership
  • Strong knowledge of site operations and trial delivery
  • Experience with CTMS platforms preferred
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