Senior Global Oncology Study Lead

IQVIA; United States; Remote; USD 93,000 - 233,000; Full time

Job summary

IQVIA Biotech is seeking a Global Study Manager to lead end-to-end planning and delivery of site management across global studies. You will oversee site activation, monitoring, and closeout while balancing speed, quality, and cost, serving as the primary client contact.

The role requires 5+ years in clinical research/monitoring, global trials experience, oncology background, and strong ICH-GCP knowledge. You will guide cross-functional teams across regions, ensuring regulatory compliance and

Qualifications

• Bachelor’s degree in life sciences or related field.
• 5+ years of clinical research/monitoring experience, including 2 years in a clinical study management role
• Strong knowledge of ICH-GCP, FDA regulations, and clinical trial processes
• Experience managing global clinical trials and multi-regional teams
• Demonstrated experience in project financial management

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

Skills

Global study management

Multi-regional experience

Phase I–III trials

Oncology experience

Therapeutic-area versatility

Education

Bachelor’s degree in life sciences or related field

Tools

CTMS

EDC

Microsoft Office

Job description

IQVIA Biotech is seeking a Global Study Manager to lead end-to-end planning and delivery of site management across global studies. You will oversee site activation, monitoring, and closeout while balancing speed, quality, and cost, serving as the primary client contact.

The role requires 5+ years in clinical research/monitoring, global trials experience, oncology background, and strong ICH-GCP knowledge. You will guide cross-functional teams across regions, ensuring regulatory compliance and