Senior Clinical Research Associate: Site Monitoring

IQVIA; Riyadh; On-site; SAR 180,000 - 240,000; Full time

Job summary

IQVIA in Riyadh, Saudi Arabia seeks an on-site Clinical Research Monitor to ensure sites conduct studies per protocol, applicable regulations and sponsor requirements. Responsibilities include performing site monitoring visits (selection, initiation, monitoring and close-out), supporting subject recruitment, administering training, maintaining TMF/ISF, and ensuring data quality and regulatory submissions.

Requirements: High School Diploma or equivalent; 2+ years on-site monitoring; GCP/ICH

Qualifications

• Knowledge of GCP/ICH guidelines.
• Experience applying regulatory requirements to clinical studies.
• Proficiency with MS Office suite.

Responsibilities

• Perform site monitoring visits (site selection, initiation, monitoring and close-out) per contract scope.
• Drive and track subject recruitment plans to support project needs.
• Administer protocol training and maintain clear communication with sites.
• Evaluate site practices for protocol compliance and regulatory adherence.
• Track regulatory submissions, recruitment, CRF completion and data queries; support startup as needed.
• Maintain TMF and ISF, submit visit reports and follow-up letters.
• Collaborate with the study team for project execution and issue resolution.

Skills

Regulatory knowledge

Communication

Time management

Relationship building

Bilingual Arabic/English

Education

High School Diploma or equivalent

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

IQVIA in Riyadh, Saudi Arabia seeks an on-site Clinical Research Monitor to ensure sites conduct studies per protocol, applicable regulations and sponsor requirements. Responsibilities include performing site monitoring visits (selection, initiation, monitoring and close-out), supporting subject recruitment, administering training, maintaining TMF/ISF, and ensuring data quality and regulatory submissions.

Requirements: High School Diploma or equivalent; 2+ years on-site monitoring; GCP/ICH