Global Oncology Study Manager – End-to-End Delivery

IQVIA; San Francisco (CA); On-site; USD 93,000 - 233,000; Full time

Job summary

IQVIA Biotech seeks a Global Study Manager to lead end-to-end site management for global trials, from activation to close-out. You will own client relationships, drive timelines, ensure ICH-GCP/regulatory compliance, and guide cross-functional teams across regions.

The role requires 5+ years in clinical research/management, Phase I–III and oncology experience, and the ability to coordinate multi-country activities across therapeutic areas.

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 manage across multiple therapeutic areas.

Responsibilities

• Lead site management strategy from study award through close-out.
• Oversee site identification, selection, activation, and recruitment.
• 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.
• Develop and manage integrated study plans and risk mitigation strategies.

Skills

Global study management

Multiregional experience

Phase I–III trials

Oncology experience

Cross-therapy collaboration

Education

Bachelor’s degree in life sciences or related field

Tools

CTMS

EDC

Microsoft Office

Job description

IQVIA Biotech seeks a Global Study Manager to lead end-to-end site management for global trials, from activation to close-out. You will own client relationships, drive timelines, ensure ICH-GCP/regulatory compliance, and guide cross-functional teams across regions.

The role requires 5+ years in clinical research/management, Phase I–III and oncology experience, and the ability to coordinate multi-country activities across therapeutic areas.