Global Oncology Trial Lead

Regulatory Jobs; Durham (NC); 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 clinical trials. You will own site activation, monitoring oversight, and closeout while balancing speed, quality, and cost.

As primary client contact, you’ll lead cross-functional teams and ensure compliance with ICH-GCP and regulatory requirements. The role requires 5+ years in clinical research/monitoring, global trial experience, and oncology exposure across multiple regions.

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.

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.

Skills

Strong communication

Cross-functional leadership

Risk management

CTMS/EDC familiarity

Education

Bachelor's degree in life sciences or related field

Tools

CTMS

EDC

MS Office

Job description

IQVIA Biotech is seeking a Global Study Manager to lead end-to-end site management for global clinical trials. You will own site activation, monitoring oversight, and closeout while balancing speed, quality, and cost.

As primary client contact, you’ll lead cross-functional teams and ensure compliance with ICH-GCP and regulatory requirements. The role requires 5+ years in clinical research/monitoring, global trial experience, and oncology exposure across multiple regions.