Director Site Operations

Greenlsr; United Kingdom; On-site; GBP 80,000 - 100,000; Full time

Job summary

A healthcare organization in the UK is seeking a Director of Site Operations to oversee the operational and strategic management of clinical research sites. The ideal candidate will have extensive experience in clinical research, particularly in leadership roles, ensuring regulatory compliance and operational excellence across multiple sites. Responsibilities include managing site partnerships, overseeing budgets, and driving performance improvements. This position offers a unique opportunity to make a significant impact in the field of clinical research.

Qualifications

• 6+ years of clinical research experience, with 3+ years in leadership.
• Strong knowledge of site operations and trial delivery.
• Experience managing clinical research site partnerships.
• Familiarity with regulatory compliance and audit readiness.

Responsibilities

• Own and manage clinical research site partnerships end-to-end.
• Lead site onboarding and ongoing operational optimisation.
• Build strong relationships with site leaders, sponsors, and internal teams.
• Oversee budgets, contracts, and financial performance.

Skills

Clinical research experience

Leadership

Site operations knowledge

CTMS platform experience

Education

Bachelor’s degree in a science-related field

Tools

CTMS

Job description

Director Site Operations – UK

About The Job

A healthcare organisation 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 optimisation
• 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

Requirements Added By The Job Poster

3+ years of work experience with Clinical Site Management

6+ years of work experience with Clinical Research

How To Apply

Send your resume and cover letter to: [e-mail]

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