Sponsor-Dedicated Clinical Research Associate (On-Site)

IQVIA; Oak Brook (IL); On-site; USD 72,000 - 189,000; Full time

Job summary

IQVIA is seeking a Clinical Site Monitor to perform site monitoring visits, ensure data integrity, and maintain regulatory compliance across assigned sites. This role focuses on driving patient recruitment plans and keeping open lines of communication with investigators to support study execution.

Based in Oak Brook, IL, the position requires experience with GCP/ICH guidelines, strong organizational skills, and proficiency with MS Office tools.

Qualifications

• Bachelor's degree in scientific discipline or healthcare preferred.
• Minimum of 2 years on-site monitoring experience.
• Knowledge of GCP/ICH guidelines and regulatory requirements.
• Proficient with MS Office and laptop/iPad usage.
• Strong written and spoken English skills.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per GCP.
• Coordinate recruitment plans with sites to support project needs.
• Administer protocol training and maintain regular site communication.
• Evaluate site practices for protocol conduct and regulatory compliance.
• Track regulatory submissions, recruitment, CRF completion and data queries.
• Ensure TMF/ISF documents are filed and maintained as required.
• Produce visit reports and follow-up letters; maintain study documentation.
• Collaborate with study team for project execution support.
• Support site recruitment planning and potential site financial management where applicable.

Skills

Written & verbal communication

Organizational skills

Problem solving

Time management

Relationship management

Education

Bachelor's degree in science or healthcare

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

IQVIA is seeking a Clinical Site Monitor to perform site monitoring visits, ensure data integrity, and maintain regulatory compliance across assigned sites. This role focuses on driving patient recruitment plans and keeping open lines of communication with investigators to support study execution.

Based in Oak Brook, IL, the position requires experience with GCP/ICH guidelines, strong organizational skills, and proficiency with MS Office tools.