Clinical Research Associate: On-site Monitoring

IQVIA; West Point (MS); On-site; USD 75,000 - 198,000; Full time

Job summary

IQVIA is seeking a Clinical Research Associate to monitor study sites in compliance with the protocol, ICH/GCP, and sponsor requirements. You will manage site visits, ensure data quality, and track regulatory submissions.

The ideal candidate has 2+ years of on-site CRA experience, strong regulatory knowledge, and excellent communication and problem-solving skills. The role requires working with sites and coordinating documentation and data queries.

Qualifications

• Bachelor's degree in scientific discipline or health care preferred.
• At least 2 years of independent on-site CRA monitoring experience.
• Good knowledge of GCP/ICH regulatory requirements.

Responsibilities

• Perform site monitoring visits (start-up, monitoring, close-out) per scope and GCP.
• Collaborate with sites to recruit and track subject enrollment and predictability.
• Administer protocol training and maintain regular communication with sites.

Skills

On-site monitoring experience

Regulatory knowledge (GCP/ICH)

Communication skills

Organizational/problem-solving

Time/financial management

Team collaboration

Education

Bachelor's degree in science/health care

Tools

EDC

CTMS

eTMF

IVRS/IWRS

Job description

IQVIA is seeking a Clinical Research Associate to monitor study sites in compliance with the protocol, ICH/GCP, and sponsor requirements. You will manage site visits, ensure data quality, and track regulatory submissions.

The ideal candidate has 2+ years of on-site CRA experience, strong regulatory knowledge, and excellent communication and problem-solving skills. The role requires working with sites and coordinating documentation and data queries.