Senior Oncology CRA - Phase 1 Trials Leader

Regulatory Jobs; Overland Park (KS); On-site; USD 72,000 - 189,000; Full time

Job summary

IQVIA seeks a Clinical Research Associate to monitor oncology sites for Phase 1 trials, ensuring GCP/ICH compliance and high data quality. You will coordinate site visits, support regulatory submissions, and mentor site staff.

A BS degree and 3+ years of oncology monitoring are required, along with strong communication and organizational skills. Join IQVIA’s global clinical research team and contribute to cutting-edge cancer investigations with a focus on patient outcomes and rigorous study

Qualifications

• BS degree required; science/healthcare preferred.
• 3+ years on-site oncology monitoring; Phase 1 experience preferred.
• Experience with GCP/ICH guidelines and regulatory requirements.

Responsibilities

• Site monitoring visits: conduct initiation, monitoring, and close-out visits per GCP/ICH.
• Support subject recruitment and track enrollment targets.
• Provide protocol training and maintain site communications.

Skills

GCP/ICH knowledge

Oncology protocol knowledge

Communication

Organization

Time management

Relationship building

Education

BS degree

Tools

MS Office

Mobile devices

Job description

IQVIA seeks a Clinical Research Associate to monitor oncology sites for Phase 1 trials, ensuring GCP/ICH compliance and high data quality. You will coordinate site visits, support regulatory submissions, and mentor site staff.

A BS degree and 3+ years of oncology monitoring are required, along with strong communication and organizational skills. Join IQVIA’s global clinical research team and contribute to cutting-edge cancer investigations with a focus on patient outcomes and rigorous study