Clinical Research Associate: Site Monitoring & Data Quality

IQVIA; O’Fallon (MO); On-site; USD 75,000 - 198,000; Full time

Job summary

IQVIA is seeking a Clinical Research Associate to perform on-site monitoring visits in accordance with GCP and protocol requirements. You will ensure site readiness, oversee data quality, and engage with sites to support recruitment and regulatory submissions.

The role requires at least 2 years of independent CRA experience, strong regulatory knowledge, and excellent communication. Proficiency with EDC/CTMS/eTMF is expected.

Qualifications

• Bachelor’s degree in a scientific field or healthcare is preferred.
• At least 2 years of on-site CRA monitoring experience in CRO/sponsor settings.
• Proficient in GCP and ICH guidelines; strong regulatory knowledge.

Responsibilities

• Perform site monitoring visits (initiation, monitoring, close-out) per scope of work and GCP.
• Coordinate subject recruitment plans with sites to enhance predictability.
• Administer protocol training and maintain regular communication with sites.

Skills

GCP knowledge

ICH guidelines knowledge

English language

Organizational skills

Time management

Communication skills

Budget/financial management

Team collaboration

Education

Bachelor's Degree in scientific discipline

Bachelor's Degree in health care

Tools

EDC

CTMS

eTMF

IVRS/IWRS

MS Word

Excel

PowerPoint

iPhone/iPad

Job description

IQVIA is seeking a Clinical Research Associate to perform on-site monitoring visits in accordance with GCP and protocol requirements. You will ensure site readiness, oversee data quality, and engage with sites to support recruitment and regulatory submissions.

The role requires at least 2 years of independent CRA experience, strong regulatory knowledge, and excellent communication. Proficiency with EDC/CTMS/eTMF is expected.