Global Oncology Study Manager — Lead Multi-Region Trials

IQVIA; Indianapolis (IN); On-site; USD 93,000 - 233,000; Full time

Job summary

IQVIA is seeking a Global Study Manager to oversee end-to-end site management for global clinical trials, balancing speed, quality and cost. You will act as the primary client contact and lead cross-functional teams to ensure site activation, monitoring, and closeout across regions.

You will drive strategic and operational excellence, ensuring compliance with ICH-GCP and regulatory standards while collaborating with sponsors, CRAs, and vendors to optimize enrollment and data quality.

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 global study site management activities.
• Serve as primary client contact and lead cross-functional teams across regions.
• Ensure site activation, monitoring oversight, and closeout in alignment with timelines and budgets.
• Coordinate with CRAs to optimize enrollment, data quality, and regulatory compliance.
• Develop and manage integrated study plans and risk mitigation strategies.
• Manage study financials, including forecasting and revenue acceleration.

Skills

Global study management

Multi-country experience

Phase I-III trials

Oncology experience

Therapeutic areas experience

Education

Bachelor’s degree in life sciences or related field

Tools

CTMS

EDC

Job description

IQVIA is seeking a Global Study Manager to oversee end-to-end site management for global clinical trials, balancing speed, quality and cost. You will act as the primary client contact and lead cross-functional teams to ensure site activation, monitoring, and closeout across regions.

You will drive strategic and operational excellence, ensuring compliance with ICH-GCP and regulatory standards while collaborating with sponsors, CRAs, and vendors to optimize enrollment and data quality.