Experienced Clinical Research Associate

Job description

If you want to take the next step as a CRA, this is your chance. You’ll receive training and development to plan and advance your career in the direction you choose, with dedicated mentoring and structured quarterly performance, promotion, and bonus reviews. Typical responsibilities include performing site selection, initiation, monitoring and close‑out visits while maintaining appropriate documentation; supporting the development of a subject recruitment plan; establishing regular communication lines and delivering protocol training to assigned sites; evaluating site practice quality and escalating issues as needed; managing progress by tracking regulatory submissions, recruitment, case report form completion and data query resolution. Collaboration and communication with diverse colleagues and customers is required, along with basic knowledge of clinical research regulatory requirements. Frequent travel to sites is required; flexibility in location with good connectivity for travel; home‑based work is possible.

Requirements

• Bachelor's degree in healthcare or scientific discipline or equivalent
• 1.5–2 years on‑site monitoring experience
• fluent in Arabic and English
• strong written and verbal communication skills with proficiency in English
• frequent travel to sites
• flexible location with good travel connectivity
• home‑based work option

Skills