Global Study Lead - Oncology Trials (Multi-Region)

IQVIA; Dallas (TX); On-site; USD 93,000 - 233,000; Full time

Job summary

IQVIA Biotech is seeking a Global Study Manager to lead end-to-end site management for global trials. You will own strategy, activation, monitoring, and closeout while ensuring speed, quality, and cost efficiency. You will be the primary client contact and lead cross-functional teams across regions.

The role requires 5+ years in clinical research with global trial experience, strong ICH-GCP knowledge, and oncology exposure. A bachelor’s degree in life sciences is required.

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, 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 meetings, including executive presentations.
• Drive collaboration across stakeholders, vendors, and functional leads.
• Develop and manage study plans and risk mitigation strategies.

Skills

Global study management

Multi-regional experience

Phase I–III trials

Oncology experience

Therapeutic versatility

Education

Bachelor’s degree in life sciences or related field

Tools

Microsoft Office

CTMS

EDC

Job description

IQVIA Biotech is seeking a Global Study Manager to lead end-to-end site management for global trials. You will own strategy, activation, monitoring, and closeout while ensuring speed, quality, and cost efficiency. You will be the primary client contact and lead cross-functional teams across regions.

The role requires 5+ years in clinical research with global trial experience, strong ICH-GCP knowledge, and oncology exposure. A bachelor’s degree in life sciences is required.