Experienced Clinical Research Associate (Multi‑Sponsored)

About the role

IQVIA is seeking an experienced Clinical Research Associate to join its multi‑sponsored projects in Saudi Arabia. You will receive structured training, mentoring, and quarterly performance reviews to support your professional growth.

Key responsibilities

• Perform site selection, initiation, monitoring, and close‑out visits while maintaining accurate documentation.
• Support the development and execution of subject recruitment plans.
• Facilitate protocol training and ongoing communication with assigned sites.
• Evaluate site practices for quality and integrity, escalating issues when necessary.
• Track regulatory submissions, recruitment metrics, CRF completion, and resolve data queries.

Required profile

• Bachelor’s degree in a health‑care or scientific discipline (or equivalent).
• 1.5–2 years of on‑site monitoring experience.
• Fluent in Arabic and English, with strong written and verbal communication skills.
• Willingness to travel frequently to study sites.

Required skills

• Clinical research regulatory requirements
• Data query resolution
• On‑site monitoring

What we offer

• Full‑time employment with a global leader in clinical research services.
• Dedicated mentoring, structured performance reviews, and clear promotion pathways.
• Flexibility to work from home while traveling to sites as needed.