Experienced Clinical Research Associate Sponsor-dedicated

Location: Riyadh, Saudi Arabia

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Conduct site selection, initiation, monitoring, and close-out visits in accordance with the protocol, Good Clinical Practice, and applicable regulations.
• Support subject recruitment planning, tracking, and enrollment activities at assigned sites.
• Train sites on study protocols and maintain regular communication to manage project expectations and issues.
• Monitor site quality, protocol compliance, regulatory submissions, CRF completion, and data query resolution.
• Maintain Trial Master File and Investigator's Site File documentation and prepare monitoring reports, follow-up letters, and action plans.
• Collaborate with study teams and, where applicable, support site financial management and invoice retrieval.

Requirements

• At least 2 years of on-site monitoring experience.
• High school diploma or equivalent; a degree in a scientific or healthcare discipline is preferred.
• Knowledge of clinical research regulations, Good Clinical Practice, and International Conference on Harmonization guidelines.
• Good therapeutic and protocol knowledge.
• Good command of Arabic and English is required.
• Proficiency with Microsoft Word, Excel, PowerPoint, laptops, and applicable mobile devices, plus strong organizational, problem-solving, communication, and time-management skills.

Culture & Benefits

• Full-time employment in a clinical research environment.
• Work involves collaboration with sites, study teams, managers, coworkers, and clients.
• Role supports the development and execution of clinical studies intended to improve medical treatments and patient outcomes.