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Northwestern University

Program Coordinator

Evanston, IL · On-site

$53K - $68K/yr

Update IS majors and minors on program requirements and targeted opportunities in collaboration with other Center for Global Studies units, the Roberta Buffett Institute, and the Global Learning ...

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As of Sep 13, 2026, the average yearly pay for masters in global studies in the United States is $100,250.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,000.00 and $130,000.00 per year, depending on experience, location, and employer.

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Infographic showing various Masters In Global Studies job openings in the United States as of August 2026, with employment types broken down into 83% Full Time, 12% Part Time, 4% Contract, and 1% Nights. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $100,250 per year, or $48.2 per hour.

Executive Director, Head of Global Site Management

Princeton, NJ • On-site

Kardigan
See more jobs at Kardiganexternal

Full-time

Re-posted 14 days ago

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 

Apply