Experienced Clinical Research Associate – Multi‑Sponsored

About the role

The Clinical Research Associate will perform monitoring and site‑management activities for multi‑sponsored studies, ensuring compliance with protocol, regulations, and sponsor requirements. This role involves close interaction with study sites to drive recruitment, maintain data quality, and support overall study execution.

Key responsibilities

• Conduct site monitoring visits (selection, initiation, monitoring, close‑out) in line with GCP and ICH guidelines.
• Work with sites to develop and track subject recruitment plans to meet project timelines.
• Provide protocol and study training to sites and maintain regular communication.
• Evaluate site practices for quality and regulatory compliance, escalating issues as needed.
• Track regulatory submissions, enrollment, CRF completion, and data query resolution.
• Maintain trial master file documentation and ensure Investigator Site Files meet GCP standards.
• Collaborate with internal study team members to support project execution.

Required profile

• Bachelor’s degree in a scientific discipline or healthcare (or equivalent education/experience).
• At least 1 year of on‑site monitoring experience.
• Fluency in English and good command of Arabic.
• Strong organizational, problem‑solving, and time‑management skills.

Required skills

• Proficiency with Microsoft Word.
• Proficiency with Microsoft Excel.
• Proficiency with Microsoft PowerPoint.
• Competence using a laptop computer and mobile devices (iPhone, iPad).