Oncology Clinical Research Associate II — Onsite Monitoring

IQVIA Inc; Durham (NC); On-site; USD 90,000 - 150,000; Full time

Job summary

IQVIA Inc. is seeking a CRA II for on-site oncology monitoring in Durham, NC. The role requires 1.5–2 years of CRA experience and hands-on site visits, with GCP/ICH compliance and strong communication with sites.

The successful candidate will manage monitoring visits, ensure TMF/ISF integrity, support recruitment plans, and collaborate with the study team to drive project success in a dynamic clinical research environment.

Qualifications

• Perform site monitoring visits (initiation, monitoring, close-out) per GCP/ICH guidelines.
• Drive subject recruitment plans in line with project needs.
• Administer protocol training and maintain regular site communications.

Responsibilities

• Maintain TMF and ISF documentation per regulatory requirements.
• Coordinate site visits and monitor CRF completion and data queries.
• Collaborate with study team to support project execution and startup phases.

Skills

On-site monitoring

GCP/ICH compliance

Site management

Education

Bachelor's Degree in scientific discipline or health care

Job description

IQVIA Inc. is seeking a CRA II for on-site oncology monitoring in Durham, NC. The role requires 1.5–2 years of CRA experience and hands-on site visits, with GCP/ICH compliance and strong communication with sites.

The successful candidate will manage monitoring visits, ensure TMF/ISF integrity, support recruitment plans, and collaborate with the study team to drive project success in a dynamic clinical research environment.