Executive Director, Head of Global Site Management

Kardigan

$150K — $200K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in life sciences or related field
  • 12+ years of experience in site management or clinical operations leadership (or advanced degree with 10+ years)
  • Deep expertise in global study start-up and enrollment optimization
  • Strong people leadership and stakeholder management skills

Responsibilities

  • Build and lead global site management and monitoring for clinical programs
  • Develop and execute site strategies for selection, activation, enrollment, and retention
  • Establish consistent monitoring models, including risk-based monitoring
  • Build and maintain strategic relationships with sites and partners
  • Work closely with various departments to ensure seamless trial execution
  • Identify and mitigate operational and quality risks at the site level
  • Establish scalable processes and metrics to track site performance
  • Create and improve standard operating procedures and ensure inspection readiness

Benefits

  • Opportunity to be part of a cutting-edge healthcare company
  • Engagement in a mission-driven organization prioritizing patient needs
  • Dynamic work environment fostering learning and innovation
  • Supportive team culture focused on collaboration and excellence
  • Opportunity to travel domestically and internationally
Full Job Description
Role Summary

The Head of Global Site Management leads all site-facing clinical trial activities across the global development portfolio. This operational leadership role is responsible for Site Management & Monitoring and Clinical Trial Optimization & Strategic Partnership functions. This role provides strategic leadership for site start-up, site management, and monitoring to drive predictable execution, accelerate timelines, improve enrollment performance, ensure high-quality data, and establish strategic site partnerships.

As a member of the Clinical Operations senior leadership team, this role is also responsible for supporting strategic initiatives across the development organization.

This is a 4 day onsite position - M-Th

Key Responsibilities
  • Build & lead global site management, monitoring, and study start-up activities across all clinical programs
  • Develop and execute site strategies to optimize selection, activation, enrollment, and retention
  • Establish consistent monitoring models, including risk-based monitoring approaches
  • Build and maintain strategic relationships with investigative sites, site networks, and partners
  • Partner closely with Clinical Operations, Clinical Development, Biometrics, and Development Services to ensure seamless, disciplined program and trial execution
  • Identify and mitigate site-level operational and quality risks
  • Establish scalable processes, metrics, and dashboards to track and improve site performance
  • Establish operating model inclusive of vendor strategy, oversight, risk management, key performance metrics, and dashboards
  • Provide expert insight into operational strategy plans (feasibility, monitoring strategies) and operating budgets
  • Create and continuously improve standard operating procedures, work instructions, to ensure inspection readiness
  • Participate in regulatory authority inspections, sponsor audits, and oversee site audits in partnership with Quality
  • Ensure compliance with GCP, regulatory requirements, and internal standards
  • Ability to assess and transform capabilities through AI and Automation solutions or strategies
  • Up to 20-30% domestic and international travel, as required.

Qualifications
  • Bachelor's degree in life sciences or related field
  • 12+ years of experience in site management or clinical operations leadership

Or advanced degree (PhD, MBA, Masters) and 10+ yrs of experience
  • Deep expertise in global study start-up and enrollment optimization
  • Strong people leadership and stakeholder management skills

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