Senior Global Oncology Study Lead

IQVIA; Gilbert (AZ); On-site; USD 93,100 - 232,800; Full time

Benefits offered by this job

Work on cutting-edge global trials

Collaborate with top talent

Impact patient outcomes worldwide

Job summary

IQVIA is seeking a Global Study Manager responsible for planning, execution, and delivery of global clinical trials. This role involves managing site selection, activation, and monitoring while ensuring compliance with regulations.

The ideal candidate will have significant experience in clinical research, especially in oncology, and will lead cross-functional teams. This role offers a competitive salary and opportunities to make a real impact in patient outcomes.

Qualifications

• 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.
• Ensure clinical monitoring processes meet study needs and timelines.
• Manage study financials, including forecasting and revenue acceleration.

Skills

Global study management experience

Experience across multiple countries

Phase I–III clinical trials experience

Oncology experience

Ability to work across multiple therapeutic areas

Education

Bachelor’s degree in life sciences or related field

Tools

Microsoft Office

Clinical systems (CTMS, EDC)

Job description

IQVIA is seeking a Global Study Manager responsible for planning, execution, and delivery of global clinical trials. This role involves managing site selection, activation, and monitoring while ensuring compliance with regulations.

The ideal candidate will have significant experience in clinical research, especially in oncology, and will lead cross-functional teams. This role offers a competitive salary and opportunities to make a real impact in patient outcomes.