Sponsor-Focused Clinical Research Associate

IQVIA; Mansfield (OH); On-site; USD 75,000 - 198,000; Full time

Job summary

IQVIA seeks a Clinical Research Associate to monitor sites and ensure data integrity for clinical studies across multiple locations. You will initiate and conduct monitoring visits, coordinate training with sites, and manage regulatory submissions, while maintaining strong communication with sponsors and internal teams.

The role requires a scientific or healthcare background, experience in GCP/ICH, and proficiency with EDC/CTMS/eTMF systems.

Qualifications

• Bachelor's degree in scientific discipline or healthcare preferred.
• Experience in on-site monitoring in CRO/sponsor setting.
• Strong knowledge of GCP/ICH guidelines and regulatory requirements.
• Proficient in Microsoft Word, Excel and PowerPoint.
• Excellent written and verbal communication in English.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring, close-out) per scope of work and GCP.
• Coordinate subject recruitment plans with sites to boost predictability.
• Deliver protocol training and maintain regular communication with sites.
• Assess site practices for protocol compliance and regulatory adherence.
• Track regulatory submissions, approvals, enrollment, CRF completion, and data query resolution.

Skills

Communication skills

English proficiency

Regulatory knowledge

MS Office (Word/Excel/PowerPoint)

Clinical trial systems (EDC/CTMS/eTMF)

Time management

Team collaboration

Problem solving

Education

Bachelor's degree in science or healthcare

Tools

EDC

CTMS

eTMF

IVRS/IWRS

Job description

IQVIA seeks a Clinical Research Associate to monitor sites and ensure data integrity for clinical studies across multiple locations. You will initiate and conduct monitoring visits, coordinate training with sites, and manage regulatory submissions, while maintaining strong communication with sponsors and internal teams.

The role requires a scientific or healthcare background, experience in GCP/ICH, and proficiency with EDC/CTMS/eTMF systems.