Oncology Clinical Research Associate II – Site Monitoring

IQVIA; Durham (NC); Remote; USD 72,000 - 182,000; Full time

Job summary

IQVIA is seeking a Clinical Research Associate (CRA) at the CRA 2 level. The role involves monitoring and site management to ensure protocol compliance and data quality across cardiovascular/renal/metabolic, oncology, and neurology studies.

Remote-friendly within the US, with onsite visits as required. The CRA will perform site monitoring visits, manage communications with sites, track regulatory submissions, and support data quality and trial documentation.

Qualifications

• Bachelor’s degree in a scientific discipline or health care preferred.
• Equivalent combination of education, training and experience may be accepted.
• Knowledge of GCP/ICH guidelines is expected.

Responsibilities

• Perform site monitoring visits in accordance with GCP/ICH and sponsor requirements.
• Drive site recruitment plans to support study timelines and predictability.
• Coordinate protocol training and maintain regular communication with sites.

Skills

Communication skills

GCP/ICH knowledge

Time management

Financial management

Education

Bachelor’s degree in science or healthcare

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

IQVIA is seeking a Clinical Research Associate (CRA) at the CRA 2 level. The role involves monitoring and site management to ensure protocol compliance and data quality across cardiovascular/renal/metabolic, oncology, and neurology studies.

Remote-friendly within the US, with onsite visits as required. The CRA will perform site monitoring visits, manage communications with sites, track regulatory submissions, and support data quality and trial documentation.