Global Study Manager - Oncology Trials Leader

IQVIA; New York (NY); On-site; USD 93,000 - 233,000; Full time

Job summary

IQVIA Global Study Manager is responsible for end-to-end planning, execution, and delivery of global clinical site management activities across studies. You will lead site activation, monitoring, and closeout while ensuring speed, quality, and cost efficiency.

You will serve as the primary client contact, steer cross-functional teams across regions, and ensure adherence to ICH-GCP, regulatory standards, and study protocols.

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 site management strategy from study award through close-out
• Oversee site identification, selection, activation, and recruitment performance
• Ensure clinical monitoring processes meet study needs and timelines
• Partner with CRAs to optimize enrollment, data quality, and compliance
• Serve as primary client contact and own key customer relationships
• Lead cross-functional teams across regions and cultures
• Facilitate internal and external meetings, including executive presentations
• Drive collaboration across stakeholders, vendors, and functional leads
• Develop and manage integrated study plans and risk mitigation strategies
• Proactively identify risks and implement corrective/preventive actions
• Monitor study timelines, enrollment trends, and data quality metrics
• Ensure compliance with GCP, SOPs, protocols, and regulatory standards
• Manage study financials, including forecasting and revenue acceleration
• Identify and manage out-of-scope work and change orders
• Oversee Billing Unit Reviews (BURs) and expense approvals
• Track performance against budget and Estimate at Completion (EAC)
• Maintain TMF health and ensure timely document submission
• Develop quality monitoring plans and compliance metrics
• Ensure adherence to study tools, training materials, and processes
• Lead and mentor cross-functional project teams
• Support CRA and team training on therapeutic areas and study-specific needs
• Foster collaboration, knowledge sharing, and continuous improvement

Skills

Global study management

Cross-regional coordination

ICH-GCP knowledge

Clinical trial processes

Budget management

Education

Bachelor’s degree in life sciences

Tools

CTMS

EDC

Microsoft Office

Job description

IQVIA Global Study Manager is responsible for end-to-end planning, execution, and delivery of global clinical site management activities across studies. You will lead site activation, monitoring, and closeout while ensuring speed, quality, and cost efficiency.

You will serve as the primary client contact, steer cross-functional teams across regions, and ensure adherence to ICH-GCP, regulatory standards, and study protocols.