Global Oncology Clinical Study Lead

IQVIA; Durham (NC); On-site; USD 93,000 - 233,000; Full time

Job summary

IQVIA is seeking a Global Study Manager to lead end-to-end site management across international trials from activation to closeout. You will be the main client contact, directing cross-functional teams and ensuring ICH-GCP compliance, timelines, and budgets across diverse regions.

The role requires 2+ years in global study management, Phase III oncology experience, and the ability to coordinate across therapeutic areas. Based in Durham, NC with global responsibilities.

Qualifications

• 2+ years of global study management experience.
• Experience across multiple countries/regions.
• Phase I–III clinical trials experience (Phase III required).
• Oncology experience required.
• Ability to work across multiple therapeutic areas.

Responsibilities

• Lead end-to-end planning, execution, and delivery of clinical trial site management across global studies.
• Serve as the primary contact for clients and lead cross-functional teams.
• Ensure compliance with ICH-GCP, regulatory requirements and study protocols.
• Oversee site activation, monitoring, and closeout while balancing speed, quality, and cost.
• Manage site identification, selection, activation, and recruitment performance.

Skills

Global study management

Multiple regions

Clinical trial coordination

Cross-functional leadership

Budget and financial oversight

Education

Bachelor’s degree in life sciences or related field

Tools

CTMS

EDC

Microsoft Office

Job description

IQVIA is seeking a Global Study Manager to lead end-to-end site management across international trials from activation to closeout. You will be the main client contact, directing cross-functional teams and ensuring ICH-GCP compliance, timelines, and budgets across diverse regions.

The role requires 2+ years in global study management, Phase III oncology experience, and the ability to coordinate across therapeutic areas. Based in Durham, NC with global responsibilities.