Clinical Research Associate – Site Monitoring & Data

IQVIA; Del Mar (CA); On-site; USD 75,000 - 198,000; Full time

Job summary

IQVIA is seeking a Clinical Research Associate (CRA) to monitor study sites and manage site-related activities to ensure compliance with the protocol and regulatory requirements. The role emphasizes on-site visits, data quality, and efficient communication with investigative sites within the United States.

Ideal candidates will have at least 2 years of on-site CRA experience, strong GCP/ICH knowledge, and proficiency with EDC/CTMS.

Qualifications

• Requires at least 2 years of on-site CRA monitoring experience in a CRO, sponsor, or similar setting.
• Good knowledge of GCP and ICH guidelines.
• Proficiency with Microsoft Word, Excel and PowerPoint.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) per scope of work and GCP.
• Track recruitment plans and enhance predictability.
• Administer protocol training and maintain communication with sites.
• Evaluate site practices for adherence to protocol and regulations; escalate issues.

Skills

Regulatory knowledge

English communication

Organizational skills

Time management

Team collaboration

Education

Bachelor's Degree in scientific discipline or health care

Tools

EDC

CTMS

eTMF

IVRS/IWRS

MS Office

Job description

IQVIA is seeking a Clinical Research Associate (CRA) to monitor study sites and manage site-related activities to ensure compliance with the protocol and regulatory requirements. The role emphasizes on-site visits, data quality, and efficient communication with investigative sites within the United States.

Ideal candidates will have at least 2 years of on-site CRA experience, strong GCP/ICH knowledge, and proficiency with EDC/CTMS.