Clinical Research Coordinator (CRC)

Roles & Responsibilities
• Coordinate and support all clinical trial activities from site initiation through close-out
• Ensure accurate and timely data entry and documentation in compliance with ICH-GCP and DOH requirements
• Assist investigators with participant screening, informed consent, and study visit procedures
• Maintain essential study documents and site files in line with Cellcolabs’ Clinical Quality Management System
• Act as the primary liaison between clinical sites, monitoring teams, and clinical operations teams
• Support monitoring visits, audits, and inspections to ensure site readiness and regulatory compliance

Qualification
• Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related field
• GCP Certification (mandatory)
• Valid UAE Driving License

Experience
• Minimum 3 years of experience in Clinical Research Coordination
• Experience in pharma, biotech, or CRO environments preferred

Skills
• Strong knowledge of ICH-GCP, DOH/IRB procedures, and ethical research conduct
• Excellent communication, organizational, and interpersonal skills
• Proficiency in English and Arabic
• Ability to work independently in a fast-paced, collaborative environment
• Strong attention to detail and compliance orientation

About the Organization
Cellcolabs is an innovative, mission-driven organization advancing regenerative medicine through high-quality clinical research. The company fosters a collaborative culture, supports professional growth, and is committed to improving patient outcomes through cutting-edge science.