Clinical Research Monitor: Site Management & Data Quality

IQVIA; Linden (NJ); On-site; USD 75,000 - 198,000; Full time

Job summary

IQVIA is seeking a Clinical Research Associate to perform on-site monitoring across multiple U.S. locations. You will ensure protocol adherence, data integrity, and regulatory compliance while coordinating site activities and training.

The role requires 2+ years of CRA experience, strong GCP/ICH knowledge, and proficiency with EDC, CTMS, eTMF, and related systems. Travel and collaboration with a global study team are core to this position.

Qualifications

• Bachelor's Degree in scientific discipline or health care preferred.
• Minimum 2 years of on-site monitoring experience as a CRA.
• Good knowledge of Good Clinical Practice (GCP) and ICH guidelines.
• Experience using EDC, CTMS, eTMF, IVRS/IWRS.
• Proficient in Microsoft Word, Excel and PowerPoint.
• Strong English communication and organizational skills.

Responsibilities

• Perform site monitoring visits per protocol and GCP.
• Coordinate subject recruitment plans with sites and project needs.
• Administer protocol training and maintain site documentation.
• Track regulatory submissions, approvals, and data queries.
• Collaborate with study team to support trial execution.

Skills

On-site monitoring

GCP/ICH knowledge

English communication

Project coordination

Regulatory awareness

Education

Bachelor's Degree in scientific discipline or health care

Tools

EDC

CTMS

eTMF

IVRS/IWRS

Microsoft Word

Microsoft Excel

PowerPoint

Job description

IQVIA is seeking a Clinical Research Associate to perform on-site monitoring across multiple U.S. locations. You will ensure protocol adherence, data integrity, and regulatory compliance while coordinating site activities and training.

The role requires 2+ years of CRA experience, strong GCP/ICH knowledge, and proficiency with EDC, CTMS, eTMF, and related systems. Travel and collaboration with a global study team are core to this position.