Clinical Research Monitor: Site Oversight & Data Quality

IQVIA; Melbourne (FL); On-site; USD 75,000 - 198,000; Full time

Job summary

IQVIA is seeking a Clinical Research Associate to perform on-site monitoring and site management across studies, ensuring data quality and regulatory compliance. You will engage with sites to drive subject recruitment, deliver protocol training, and maintain open lines of communication to manage project expectations.

The role requires a minimum of 2 years of independent CRA experience, solid GCP/ICH knowledge, and proficiency with EDC, CTMS, and eTMF systems.

Qualifications

• Bachelor's degree in scientific discipline or health care preferred.
• At least 2 years on-site CRA experience in a CRO, sponsor, or similar setting.
• Good knowledge of GCP and ICH guidelines.
• Proficient in Microsoft Word, Excel and PowerPoint; comfortable with laptops and mobile devices.
• Experience using EDC, CTMS, eTMF and IVRS/IWRS.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per scope of work and GCP.
• Drive and track subject recruitment to align with project needs.
• Administer protocol training and establish regular communication with sites.
• Evaluate site practices for protocol adherence and regulatory compliance.
• Track regulatory submissions, recruitment, CRF completion, and data queries.

Skills

On-site monitoring

GCP & ICH knowledge

English communication

Time management

Organizational skills

Financial management

Team collaboration

Education

Bachelor's Degree in science or healthcare

Tools

EDC

CTMS

eTMF

IVRS/IWRS

Job description

IQVIA is seeking a Clinical Research Associate to perform on-site monitoring and site management across studies, ensuring data quality and regulatory compliance. You will engage with sites to drive subject recruitment, deliver protocol training, and maintain open lines of communication to manage project expectations.

The role requires a minimum of 2 years of independent CRA experience, solid GCP/ICH knowledge, and proficiency with EDC, CTMS, and eTMF systems.